Atrial FibrillationPhase 3NCT00808067
RELY-ABLE Long Term Multi-center Extension of Dabigatran Treatment in Patients With Atrial Fibrillation Who Completed RE-LY Trial
A Phase 3 study testing dabigatran dose 1 and dabigatran dose 2 in people with Atrial Fibrillation, run by Boehringer Ingelheim at 567 sites in 35 countries.
Trial summary
The purposes of this study are: 1. To evaluate the long-term safety of dabigatran etexilate 2. To assess the effect of a knowledge translation intervention on patient outcomes Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Atrial Fibrillation
- What is being tested?
- dabigatran dose 1 and dabigatran dose 2
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 5,897 participants
- Where
- 567 sitesin 35 countries
- Study dates
- Nov 2008to Dec 2012
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Participation in RE-LY, requires long term anticoagulation, provides written informed consent
Who cannot join
- Permanent discontinuation of dabigatran during RE-LY
Trial locations and contacts
567 sites in 35 countries.
567 sites in 35 countries
United States216 sites
1160.71.0203 Boehringer Ingelheim Investigational Site
Akron, Ohio
1160.71.0476 Boehringer Ingelheim Investigational Site
Albany, New York
1160.71.0301 Boehringer Ingelheim Investigational Site
Allentown, Pennsylvania
1160.71.0114 Boehringer Ingelheim Investigational Site
Annapolis, Maryland
1160.71.0353 Boehringer Ingelheim Investigational Site
Asheville, North Carolina
1160.71.0159 Boehringer Ingelheim Investigational Site
Atlanta, Georgia
1160.71.0096 Boehringer Ingelheim Investigational Site
Auburn, Maine
1160.71.0021 Boehringer Ingelheim Investigational Site
Augusta, Georgia
1160.71.0129 Boehringer Ingelheim Investigational Site
Austin, Texas
1160.71.0410 Boehringer Ingelheim Investigational Site
Austin, Texas
1160.71.0023 Boehringer Ingelheim Investigational Site
Baltimore, Maryland
1160.71.0047 Boehringer Ingelheim Investigational Site
Baltimore, Maryland
1160.71.0079 Boehringer Ingelheim Investigational Site
Baltimore, Maryland
1160.71.0186 Boehringer Ingelheim Investigational Site
Baltimore, Maryland
1160.71.0194 Boehringer Ingelheim Investigational Site
Baltimore, Maryland
1160.71.0144 Boehringer Ingelheim Investigational Site
Baton Rouge, Louisiana
1160.71.0007 Boehringer Ingelheim Investigational Site
Beaufort, South Carolina
1160.71.0255 Boehringer Ingelheim Investigational Site
Bel Air, Maryland
1160.71.0050 Boehringer Ingelheim Investigational Site
Bellingham, Washington
1160.71.0046 Boehringer Ingelheim Investigational Site
Birmingham, Alabama
1160.71.0057 Boehringer Ingelheim Investigational Site
Birmingham, Alabama
1160.71.0211 Boehringer Ingelheim Investigational Site
Birmingham, Alabama
1160.71.0382 Boehringer Ingelheim Investigational Site
Boynton Beach, Florida
1160.71.0056 Boehringer Ingelheim Investigational Site
Brandon, Florida
1160.71.0278 Boehringer Ingelheim Investigational Site
Bridgeport, Connecticut
1160.71.0142 Boehringer Ingelheim Investigational Site
Browns Mills, New Jersey
1160.71.0040 Boehringer Ingelheim Investigational Site
Burien, Washington
1160.71.0295 Boehringer Ingelheim Investigational Site
Camp Hill, Pennsylvania
1160.71.0434 Boehringer Ingelheim Investigational Site
Canal Fulton, Ohio
1160.71.0441 Boehringer Ingelheim Investigational Site
Carmichael, California
1160.71.0383 Boehringer Ingelheim Investigational Site
Charleston, South Carolina
1160.71.0080 Boehringer Ingelheim Investigational Site
Charlotte, North Carolina
1160.71.0453 Boehringer Ingelheim Investigational Site
Charlottesville, Virginia
1160.71.0084 Boehringer Ingelheim Investigational Site
Chattanooga, Tennessee
1160.71.0221 Boehringer Ingelheim Investigational Site
Cherry Hill, New Jersey
1160.71.0053 Boehringer Ingelheim Investigational Site
Chesapeake, Virginia
1160.71.0218 Boehringer Ingelheim Investigational Site
Cicero, Illinois
1160.71.0402 Boehringer Ingelheim Investigational Site
Cincinnati, Ohio
1160.71.0426 Boehringer Ingelheim Investigational Site
Cincinnati, Ohio
1160.71.0479 Boehringer Ingelheim Investigational Site
Cincinnati, Ohio
1160.71.0169 Boehringer Ingelheim Investigational Site
Clarksburg, West Virginia
1160.71.0296 Boehringer Ingelheim Investigational Site
Clearwater, Florida
1160.71.0263 Boehringer Ingelheim Investigational Site
Cleveland, Ohio
1160.71.0480 Boehringer Ingelheim Investigational Site
Cleveland, Ohio
1160.71.0474 Boehringer Ingelheim Investigational Site
Clinton, Tennessee
1160.71.0321 Boehringer Ingelheim Investigational Site
Colorado Springs, Colorado
1160.71.0449 Boehringer Ingelheim Investigational Site
Colorado Springs, Colorado
1160.71.0398 Boehringer Ingelheim Investigational Site
Columbia, Maryland
1160.71.0055 Boehringer Ingelheim Investigational Site
Columbia, Missouri
1160.71.0267 Boehringer Ingelheim Investigational Site
Columbus, Ohio
1160.71.0161 Boehringer Ingelheim Investigational Site
Conyers, Georgia
1160.71.0327 Boehringer Ingelheim Investigational Site
Coral Springs, Florida
1160.71.0044 Boehringer Ingelheim Investigational Site
Cortlandt Manor, New York
1160.71.0139 Boehringer Ingelheim Investigational Site
Corvallis, Oregon
1160.71.0156 Boehringer Ingelheim Investigational Site
Dallas, Texas
1160.71.0035 Boehringer Ingelheim Investigational Site
Dayton, Ohio
1160.71.0376 Boehringer Ingelheim Investigational Site
Daytona Beach, Florida
1160.71.0360 Boehringer Ingelheim Investigational Site
Denver, Colorado
1160.71.0413 Boehringer Ingelheim Investigational Site
Denver, Colorado
1160.71.0268 Boehringer Ingelheim Investigational Site
Dubuque, Iowa
1160.71.0325 Boehringer Ingelheim Investigational Site
Eugene, Oregon
1160.71.0150 Boehringer Ingelheim Investigational Site
Fairview Park, Ohio
1160.71.0248 Boehringer Ingelheim Investigational Site
Flemington, New Jersey
1160.71.0362 Boehringer Ingelheim Investigational Site
Fort Collins, Colorado
1160.71.0074 Boehringer Ingelheim Investigational Site
Fort Myers, Florida
1160.71.0377 Boehringer Ingelheim Investigational Site
Fort Wayne, Indiana
1160.71.0315 Boehringer Ingelheim Investigational Site
Fort Worth, Texas
1160.71.0428 Boehringer Ingelheim Investigational Site
Fredericksburg, Virginia
1160.71.0333 Boehringer Ingelheim Investigational Site
Fullerton, California
1160.71.0350 Boehringer Ingelheim Investigational Site
Gastonia, North Carolina
1160.71.0062 Boehringer Ingelheim Investigational Site
Germantown, Tennessee
1160.71.0154 Boehringer Ingelheim Investigational Site
Grand Blanc, Michigan
1160.71.0102 Boehringer Ingelheim Investigational Site
Grand Forks, North Dakota
1160.71.0313 Boehringer Ingelheim Investigational Site
Greenville, South Carolina
1160.71.0482 Boehringer Ingelheim Investigational Site
Guilford, Connecticut
1160.71.0086 Boehringer Ingelheim Investigational Site
Gulfport, Mississippi
1160.71.0311 Boehringer Ingelheim Investigational Site
Harrisonburg, Virginia
1160.71.0443 Boehringer Ingelheim Investigational Site
Haverhill, Massachusetts
1160.71.0452 Boehringer Ingelheim Investigational Site
Haverhill, Massachusetts
1160.71.0346 Boehringer Ingelheim Investigational Site
Henderson, Nevada
1160.71.0294 Boehringer Ingelheim Investigational Site
Hershey, Pennsylvania
1160.71.0173 Boehringer Ingelheim Investigational Site
High Point, North Carolina
1160.71.0038 Boehringer Ingelheim Investigational Site
Hot Springs, Arkansas
1160.71.0447 Boehringer Ingelheim Investigational Site
Houston, Texas
1160.71.0365 Boehringer Ingelheim Investigational Site
Huntington, West Virginia
1160.71.0288 Boehringer Ingelheim Investigational Site
Indianapolis, Indiana
1160.71.0352 Boehringer Ingelheim Investigational Site
Indianapolis, Indiana
1160.71.0436 Boehringer Ingelheim Investigational Site
Indianapolis, Indiana
1160.71.0089 Boehringer Ingelheim Investigational Site
Jacksonville, Florida
1160.71.0232 Boehringer Ingelheim Investigational Site
Jacksonville, Florida
1160.71.0427 Boehringer Ingelheim Investigational Site
Jacksonville, Florida
1160.71.0222 Boehringer Ingelheim Investigational Site
Jamestown, North Dakota
1160.71.0369 Boehringer Ingelheim Investigational Site
Jenkintown, Pennsylvania
1160.71.0370 Boehringer Ingelheim Investigational Site
Johnson City, Tennessee
1160.71.0302 Boehringer Ingelheim Investigational Site
Jonesboro, Arkansas
1160.71.0027 Boehringer Ingelheim Investigational Site
Kalispell, Montana
1160.71.0257 Boehringer Ingelheim Investigational Site
Kansas City, Missouri
1160.71.0201 Boehringer Ingelheim Investigational Site
Kettering, Ohio
1160.71.0483 Boehringer Ingelheim Investigational Site
Killeen, Texas
1160.71.0384 Boehringer Ingelheim Investigational Site
La Jolla, California
1160.71.0018 Boehringer Ingelheim Investigational Site
Lafayette, Louisiana
1160.71.0104 Boehringer Ingelheim Investigational Site
Lake Havasu City, Arizona
1160.71.0012 Boehringer Ingelheim Investigational Site
Lakeland, Florida
1160.71.0246 Boehringer Ingelheim Investigational Site
Lancaster, California
1160.71.0431 Boehringer Ingelheim Investigational Site
Lancaster, Pennsylvania
1160.71.0168 Boehringer Ingelheim Investigational Site
Langhorne, Pennsylvania
1160.71.0205 Boehringer Ingelheim Investigational Site
Lapeer, Michigan
1160.71.0430 Boehringer Ingelheim Investigational Site
Las Vegas, Nevada
1160.71.0422 Boehringer Ingelheim Investigational Site
Lexington, Kentucky
1160.71.0191 Boehringer Ingelheim Investigational Site
Little Rock, Arkansas
1160.71.0213 Boehringer Ingelheim Investigational Site
Little Rock, Arkansas
1160.71.0223 Boehringer Ingelheim Investigational Site
Lorain, Ohio
1160.71.0178 Boehringer Ingelheim Investigational Site
Louisville, Kentucky
1160.71.0397 Boehringer Ingelheim Investigational Site
Louisville, Kentucky
1160.71.0335 Boehringer Ingelheim Investigational Site
Lubbock, Texas
1160.71.0214 Boehringer Ingelheim Investigational Site
Lyndhurst, Ohio
1160.71.0099 Boehringer Ingelheim Investigational Site
Madison, Wisconsin
1160.71.0438 Boehringer Ingelheim Investigational Site
Maywood, Illinois
1160.71.0293 Boehringer Ingelheim Investigational Site
Meadowbrook, Pennsylvania
1160.71.0331 Boehringer Ingelheim Investigational Site
Melrose Park, Illinois
1160.71.0070 Boehringer Ingelheim Investigational Site
Merced, California
1160.71.0034 Boehringer Ingelheim Investigational Site
Miami, Florida
1160.71.0072 Boehringer Ingelheim Investigational Site
Milwaukee, Wisconsin
1160.71.0461 Boehringer Ingelheim Investigational Site
Milwaukee, Wisconsin
1160.71.0229 Boehringer Ingelheim Investigational Site
Mineola, New York
1160.71.0451 Boehringer Ingelheim Investigational Site
Mineola, New York
1160.71.0202 Boehringer Ingelheim Investigational Site
Minneapolis, Minnesota
1160.71.0115 Boehringer Ingelheim Investigational Site
Mobile, Alabama
1160.71.0279 Boehringer Ingelheim Investigational Site
Muskegon, Michigan
1160.71.0395 Boehringer Ingelheim Investigational Site
Nashville, Tennessee
1160.71.0029 Boehringer Ingelheim Investigational Site
Natick, Massachusetts
1160.71.0132 Boehringer Ingelheim Investigational Site
New Iberia, Louisiana
1160.71.0183 Boehringer Ingelheim Investigational Site
New Rochelle, New York
1160.71.0292 Boehringer Ingelheim Investigational Site
Newport News, Virginia
1160.71.0364 Boehringer Ingelheim Investigational Site
Normal, Illinois
1160.71.0394 Boehringer Ingelheim Investigational Site
Norristown, Pennsylvania
1160.71.0109 Boehringer Ingelheim Investigational Site
North Chicago, Illinois
1160.71.0003 Boehringer Ingelheim Investigational Site
North Dartmouth, Massachusetts
1160.71.0210 Boehringer Ingelheim Investigational Site
Northport, New York
1160.71.0152 Boehringer Ingelheim Investigational Site
Oak Lawn, Illinois
1160.71.0349 Boehringer Ingelheim Investigational Site
Oakland, California
1160.71.0478 Boehringer Ingelheim Investigational Site
Oakland, New Jersey
1160.71.0392 Boehringer Ingelheim Investigational Site
Ocean City, New Jersey
1160.71.0016 Boehringer Ingelheim Investigational Site
Oceanside, California
1160.71.0110 Boehringer Ingelheim Investigational Site
Omaha, Nebraska
1160.71.0227 Boehringer Ingelheim Investigational Site
Orlando, Florida
1160.71.0095 Boehringer Ingelheim Investigational Site
Ormond Beach, Florida
1160.71.0310 Boehringer Ingelheim Investigational Site
Owensboro, Kentucky
1160.71.0459 Boehringer Ingelheim Investigational Site
Pasadena, California
1160.71.0037 Boehringer Ingelheim Investigational Site
Pensacola, Florida
1160.71.0445 Boehringer Ingelheim Investigational Site
Petoskey, Michigan
1160.71.0006 Boehringer Ingelheim Investigational Site
Pinehurst, North Carolina
1160.71.0466 Boehringer Ingelheim Investigational Site
Pittsburgh, Pennsylvania
1160.71.0137 Boehringer Ingelheim Investigational Site
Port Charlotte, Florida
1160.71.0417 Boehringer Ingelheim Investigational Site
Port Charlotte, Florida
1160.71.0075 Boehringer Ingelheim Investigational Site
Poughkeepsie, New York
1160.71.0270 Boehringer Ingelheim Investigational Site
Poway, California
1160.71.0135 Boehringer Ingelheim Investigational Site
Riverside, California
1160.71.0274 Boehringer Ingelheim Investigational Site
Rochester Hills, Michigan
1160.71.0198 Boehringer Ingelheim Investigational Site
Rockford, Illinois
1160.71.0332 Boehringer Ingelheim Investigational Site
Rockledge, Florida
1160.71.0177 Boehringer Ingelheim Investigational Site
Rockville, Maryland
1160.71.0300 Boehringer Ingelheim Investigational Site
Sacramento, California
1160.71.0165 Boehringer Ingelheim Investigational Site
Saginaw, Michigan
1160.71.0336 Boehringer Ingelheim Investigational Site
Saint Charles, Missouri
1160.71.0101 Boehringer Ingelheim Investigational Site
Saint Paul, Minnesota
1160.71.0220 Boehringer Ingelheim Investigational Site
Salem, Virginia
1160.71.0073 Boehringer Ingelheim Investigational Site
Salisbury, Maryland
1160.71.0207 Boehringer Ingelheim Investigational Site
Salisbury, Maryland
1160.71.0269 Boehringer Ingelheim Investigational Site
San Antonio, Texas
1160.71.0307 Boehringer Ingelheim Investigational Site
San Antonio, Texas
1160.71.0284 Boehringer Ingelheim Investigational Site
San Diego, California
1160.71.0285 Boehringer Ingelheim Investigational Site
San Marcos, Texas
1160.71.0275 Boehringer Ingelheim Investigational Site
Sandusky, Ohio
1160.71.0385 Boehringer Ingelheim Investigational Site
Sarasota, Florida
1160.71.0208 Boehringer Ingelheim Investigational Site
Sellersville, Pennsylvania
1160.71.0235 Boehringer Ingelheim Investigational Site
South Bend, Indiana
1160.71.0166 Boehringer Ingelheim Investigational Site
Spartanburg, South Carolina
1160.71.0250 Boehringer Ingelheim Investigational Site
Spokane, Washington
1160.71.0133 Boehringer Ingelheim Investigational Site
Springfield, Oregon
1160.71.0249 Boehringer Ingelheim Investigational Site
St Louis, Missouri
1160.71.0015 Boehringer Ingelheim Investigational Site
St. Petersburg, Florida
1160.71.0339 Boehringer Ingelheim Investigational Site
St. Petersburg, Florida
1160.71.0002 Boehringer Ingelheim Investigational Site
Statesville, North Carolina
1160.71.0069 Boehringer Ingelheim Investigational Site
Statesville, North Carolina
1160.71.0224 Boehringer Ingelheim Investigational Site
Suffolk, Virginia
1160.71.0008 Boehringer Ingelheim Investigational Site
Summerville, South Carolina
1160.71.0256 Boehringer Ingelheim Investigational Site
Tacoma, Washington
1160.71.0196 Boehringer Ingelheim Investigational Site
Takoma Park, Maryland
1160.71.0113 Boehringer Ingelheim Investigational Site
The Bronx, New York
1160.71.0281 Boehringer Ingelheim Investigational Site
The Bronx, New York
1160.71.0187 Boehringer Ingelheim Investigational Site
Towson, Maryland
1160.71.0020 Boehringer Ingelheim Investigational Site
Troy, Michigan
1160.71.0414 Boehringer Ingelheim Investigational Site
Troy, New York
1160.71.0185 Boehringer Ingelheim Investigational Site
Tucson, Arizona
1160.71.0435 Boehringer Ingelheim Investigational Site
Tulsa, Oklahoma
1160.71.0119 Boehringer Ingelheim Investigational Site
Tupelo, Mississippi
1160.71.0367 Boehringer Ingelheim Investigational Site
Tyler, Texas
1160.71.0465 Boehringer Ingelheim Investigational Site
Uniontown, Pennsylvania
1160.71.0019 Boehringer Ingelheim Investigational Site
Vero Beach, Florida
1160.71.0379 Boehringer Ingelheim Investigational Site
Walnut Creek, California
1160.71.0356 Boehringer Ingelheim Investigational Site
Watertown, New York
1160.71.0024 Boehringer Ingelheim Investigational Site
Wenatchee, Washington
1160.71.0001 Boehringer Ingelheim Investigational Site
West Des Moines, Iowa
1160.71.0357 Boehringer Ingelheim Investigational Site
West Des Moines, Iowa
1160.71.0103 Boehringer Ingelheim Investigational Site
Westlake, Ohio
1160.71.0052 Boehringer Ingelheim Investigational Site
Westminster, Maryland
1160.71.0254 Boehringer Ingelheim Investigational Site
Westwood, New Jersey
1160.71.0317 Boehringer Ingelheim Investigational Site
Winchester, Virginia
1160.71.0433 Boehringer Ingelheim Investigational Site
Winfield, Illinois
1160.71.0472 Boehringer Ingelheim Investigational Site
Woodland Park, New Jersey
1160.71.0308 Boehringer Ingelheim Investigational Site
Worcester, Massachusetts
1160.71.0032 Boehringer Ingelheim Investigational Site
Wynnewood, Pennsylvania
1160.71.0067 Boehringer Ingelheim Investigational Site
Wyomissing, Pennsylvania
1160.71.0064 Boehringer Ingelheim Investigational Site
Yonkers, New York
1160.71.0188 Boehringer Ingelheim Investigational Site
Ypsilanti, Michigan
Canada40 sites
1160.71.0674 Boehringer Ingelheim Investigational Site
Burlington, Ontario
1160.71.0694 Boehringer Ingelheim Investigational Site
Calgary, Alberta
1160.71.0696 Boehringer Ingelheim Investigational Site
Calgary, Alberta
1160.71.0702 Boehringer Ingelheim Investigational Site
Cambridge, Ontario
1160.71.0720 Boehringer Ingelheim Investigational Site
Cambridge, Ontario
1160.71.0680 Boehringer Ingelheim Investigational Site
Coquitlam, British Columbia
1160.71.0712 Boehringer Ingelheim Investigational Site
Coquitlam, British Columbia
1160.71.0715 Boehringer Ingelheim Investigational Site
Greater Sudbury, Ontario
1160.71.0692 Boehringer Ingelheim Investigational Site
Grimsby, Ontario
1160.71.0703 Boehringer Ingelheim Investigational Site
Halifax, Nova Scotia
1160.71.0697 Boehringer Ingelheim Investigational Site
Hamilton, Ontario
1160.71.0710 Boehringer Ingelheim Investigational Site
Hamilton, Ontario
1160.71.0719 Boehringer Ingelheim Investigational Site
Hamilton, Ontario
1160.71.0721 Boehringer Ingelheim Investigational Site
Hamilton, Ontario
1160.71.0706 Boehringer Ingelheim Investigational Site
Kelowna, British Columbia
1160.71.0708 Boehringer Ingelheim Investigational Site
Mississauga, Ontario
1160.71.0683 Boehringer Ingelheim Investigational Site
Montreal, Quebec
1160.71.0705 Boehringer Ingelheim Investigational Site
Montreal, Quebec
1160.71.0709 Boehringer Ingelheim Investigational Site
Montreal, Quebec
1160.71.0716 Boehringer Ingelheim Investigational Site
Montreal, Quebec
1160.71.0725 Boehringer Ingelheim Investigational Site
Nanaimo, British Columbia
1160.71.0691 Boehringer Ingelheim Investigational Site
New Westminster, British Columbia
1160.71.0688 Boehringer Ingelheim Investigational Site
Newmarket, Ontario
1160.71.0672 Boehringer Ingelheim Investigational Site
Oshawa, Ontario
1160.71.0687 Boehringer Ingelheim Investigational Site
Ottawa, Ontario
1160.71.0701 Boehringer Ingelheim Investigational Site
Portage la Prairie, Manitoba
1160.71.0700 Boehringer Ingelheim Investigational Site
Québec, Quebec
1160.71.0717 Boehringer Ingelheim Investigational Site
Québec, Quebec
1160.71.0713 Boehringer Ingelheim Investigational Site
Saint George-de-Beauce, Quebec
1160.71.0699 Boehringer Ingelheim Investigational Site
Saint-Charles-Borromée, Quebec
1160.71.0675 Boehringer Ingelheim Investigational Site
Saint-Hyacinthe, Quebec
1160.71.0673 Boehringer Ingelheim Investigational Site
Saskatoon, Saskatchewan
1160.71.0678 Boehringer Ingelheim Investigational Site
Saskatoon, Saskatchewan
1160.71.0679 Boehringer Ingelheim Investigational Site
Scarborough Village, Ontario
1160.71.0723 Boehringer Ingelheim Investigational Site
Scarborough Village, Ontario
1160.71.0690 Boehringer Ingelheim Investigational Site
Thunder Bay, Ontario
1160.71.0684 Boehringer Ingelheim Investigational Site
Toronto, Ontario
1160.71.0718 Boehringer Ingelheim Investigational Site
Toronto, Ontario
1160.71.0714 Boehringer Ingelheim Investigational Site
Victoria, British Columbia
1160.71.0686 Boehringer Ingelheim Investigational Site
Windsor, Ontario
Netherlands27 sites
1160.71.1337 Boehringer Ingelheim Investigational Site
's-Hertogenbosch
1160.71.1344 Boehringer Ingelheim Investigational Site
Almelo
1160.71.1331 Boehringer Ingelheim Investigational Site
Amsterdam
1160.71.1336 Boehringer Ingelheim Investigational Site
Apeldoorn
1160.71.1332 Boehringer Ingelheim Investigational Site
Breda
1160.71.1349 Boehringer Ingelheim Investigational Site
Den Helder
1160.71.1345 Boehringer Ingelheim Investigational Site
Deventer
1160.71.1360 Boehringer Ingelheim Investigational Site
Dirksland
1160.71.1340 Boehringer Ingelheim Investigational Site
Ede
1160.71.1358 Boehringer Ingelheim Investigational Site
Eindhoven
1160.71.1338 Boehringer Ingelheim Investigational Site
Enschede
1160.71.1343 Boehringer Ingelheim Investigational Site
Goes
1160.71.1347 Boehringer Ingelheim Investigational Site
Gorinchem
1160.71.1333 Boehringer Ingelheim Investigational Site
Groningen
1160.71.1361 Boehringer Ingelheim Investigational Site
Heerlen
1160.71.1339 Boehringer Ingelheim Investigational Site
Hengelo
1160.71.1346 Boehringer Ingelheim Investigational Site
Hilversum
1160.71.1356 Boehringer Ingelheim Investigational Site
Hoorn
1160.71.1359 Boehringer Ingelheim Investigational Site
Maastricht
1160.71.1341 Boehringer Ingelheim Investigational Site
Meppel
1160.71.1354 Boehringer Ingelheim Investigational Site
Rotterdam
1160.71.1351 Boehringer Ingelheim Investigational Site
Sneek
1160.71.1353 Boehringer Ingelheim Investigational Site
Tiel
1160.71.1352 Boehringer Ingelheim Investigational Site
Tilburg
1160.71.1350 Boehringer Ingelheim Investigational Site
Veldhoven
1160.71.1342 Boehringer Ingelheim Investigational Site
Velp
1160.71.1348 Boehringer Ingelheim Investigational Site
Zwijndrecht
France26 sites
1160.71.875A Boehringer Ingelheim Investigational Site
Abbeville
1160.71.882D Boehringer Ingelheim Investigational Site
Angers
1160.71.882G Boehringer Ingelheim Investigational Site
Angers
1160.71.879F Boehringer Ingelheim Investigational Site
Besle Sur Vilaine
1160.71.882K Boehringer Ingelheim Investigational Site
Château-Gontier
1160.71.887A Boehringer Ingelheim Investigational Site
Cholet
1160.71.879C Boehringer Ingelheim Investigational Site
Derval
1160.71.882H Boehringer Ingelheim Investigational Site
Feneu
1160.71.888A Boehringer Ingelheim Investigational Site
Grenoble Cédex 9
1160.71.879B Boehringer Ingelheim Investigational Site
La Chapelle-sur-Erdre
1160.71.874A Boehringer Ingelheim Investigational Site
Langres
1160.71.884A Boehringer Ingelheim Investigational Site
Laval
1160.71.880B Boehringer Ingelheim Investigational Site
Le Mesnil En Valée
1160.71.880A Boehringer Ingelheim Investigational Site
Mûrs-Erigné
1160.71.879A Boehringer Ingelheim Investigational Site
Nantes
1160.71.879H Boehringer Ingelheim Investigational Site
Nantes
1160.71.879S Boehringer Ingelheim Investigational Site
Nantes
1160.71.880J Boehringer Ingelheim Investigational Site
Parçay-les-Pins
1160.71.871A Boehringer Ingelheim Investigational Site
Paris
1160.71.879E Boehringer Ingelheim Investigational Site
Saint-Aubin-des-Châteaux
1160.71.880D Boehringer Ingelheim Investigational Site
Segré
1160.71.882A Boehringer Ingelheim Investigational Site
Tiercé
1160.71.882B Boehringer Ingelheim Investigational Site
Tiercé
1160.71.882C Boehringer Ingelheim Investigational Site
Tiercé
1160.71.879G Boehringer Ingelheim Investigational Site
Vieillevigne
1160.71.880E Boehringer Ingelheim Investigational Site
Vihiers
Israel26 sites
1160.71.1110 Boehringer Ingelheim Investigational Site
Afula
1160.71.1121 Boehringer Ingelheim Investigational Site
Afula
1160.71.1111 Boehringer Ingelheim Investigational Site
Ashkelon
1160.71.1117 Boehringer Ingelheim Investigational Site
Giv‘atayim
1160.71.1112 Boehringer Ingelheim Investigational Site
Hadera
1160.71.1091 Boehringer Ingelheim Investigational Site
Haifa
1160.71.1113 Boehringer Ingelheim Investigational Site
Haifa
1160.71.1114 Boehringer Ingelheim Investigational Site
Haifa
1160.71.1116 Boehringer Ingelheim Investigational Site
Haifa
1160.71.1118 Boehringer Ingelheim Investigational Site
Haifa
1160.71.1105 Boehringer Ingelheim Investigational Site
Holon
1160.71.1101 Boehringer Ingelheim Investigational Site
Jerusalem
1160.71.1104 Boehringer Ingelheim Investigational Site
Jerusalem
1160.71.1106 Boehringer Ingelheim Investigational Site
Jerusalem
1160.71.1119 Boehringer Ingelheim Investigational Site
Kfar Saba
1160.71.1096 Boehringer Ingelheim Investigational Site
Petah Tikva
1160.71.1093 Boehringer Ingelheim Investigational Site
Ramat Gan
1160.71.1094 Boehringer Ingelheim Investigational Site
Ramat Gan
1160.71.1095 Boehringer Ingelheim Investigational Site
Ramat Gan
1160.71.1100 Boehringer Ingelheim Investigational Site
Rehovot
1160.71.1103 Boehringer Ingelheim Investigational Site
Safed
1160.71.1107 Boehringer Ingelheim Investigational Site
Tel Aviv
1160.71.1108 Boehringer Ingelheim Investigational Site
Tel Aviv
1160.71.1109 Boehringer Ingelheim Investigational Site
Tel Aviv
1160.71.1120 Boehringer Ingelheim Investigational Site
Tel Aviv
1160.71.1122 Boehringer Ingelheim Investigational Site
Tel Aviv
Belgium17 sites
1160.71.0564 Boehringer Ingelheim Investigational Site
Aalst
1160.71.0572 Boehringer Ingelheim Investigational Site
Brasschaat
1160.71.0571 Boehringer Ingelheim Investigational Site
Brussels
1160.71.0581 Boehringer Ingelheim Investigational Site
Brussels
1160.71.0585 Boehringer Ingelheim Investigational Site
Brussels
1160.71.0563 Boehringer Ingelheim Investigational Site
Edegem
1160.71.0578 Boehringer Ingelheim Investigational Site
Genk
1160.71.0587 Boehringer Ingelheim Investigational Site
Genk
1160.71.0574 Boehringer Ingelheim Investigational Site
Ghent
1160.71.0588 Boehringer Ingelheim Investigational Site
Gilly
1160.71.0568 Boehringer Ingelheim Investigational Site
Hasselt
1160.71.0561 Boehringer Ingelheim Investigational Site
Leuven
1160.71.0579 Boehringer Ingelheim Investigational Site
Liège
1160.71.0567 Boehringer Ingelheim Investigational Site
Ostend
1160.71.0570 Boehringer Ingelheim Investigational Site
Roeselare
1160.71.0566 Boehringer Ingelheim Investigational Site
Tienen
1160.71.0562 Boehringer Ingelheim Investigational Site
Turnhout
Germany17 sites
1160.71.0932 Boehringer Ingelheim Investigational Site
Berlin
1160.71.0948 Boehringer Ingelheim Investigational Site
Berlin
1160.71.0962 Boehringer Ingelheim Investigational Site
Berlin
1160.71.0940 Boehringer Ingelheim Investigational Site
Bochum
1160.71.0963 Boehringer Ingelheim Investigational Site
Cologne
1160.71.0972 Boehringer Ingelheim Investigational Site
Dortmund
1160.71.0934 Boehringer Ingelheim Investigational Site
Essen
1160.71.0931 Boehringer Ingelheim Investigational Site
Frankfurt am Main
1160.71.0943 Boehringer Ingelheim Investigational Site
Heidelberg
1160.71.0946 Boehringer Ingelheim Investigational Site
Lahr
1160.71.0944 Boehringer Ingelheim Investigational Site
Limburg
1160.71.0951 Boehringer Ingelheim Investigational Site
Mainz
1160.71.0933 Boehringer Ingelheim Investigational Site
Mannheim
1160.71.0945 Boehringer Ingelheim Investigational Site
Mannheim
1160.71.0970 Boehringer Ingelheim Investigational Site
Mannheim
1160.71.0937 Boehringer Ingelheim Investigational Site
Witten
1160.71.0966 Boehringer Ingelheim Investigational Site
Wuppertal
India13 sites
1160.71.1057 Boehringer Ingelheim Investigational Site
Ahmedabad
1160.71.1056 Boehringer Ingelheim Investigational Site
Ahmedabad-52
1160.71.1065 Boehringer Ingelheim Investigational Site
Bangalore
1160.71.1062 Boehringer Ingelheim Investigational Site
Hyderabad
1160.71.1073 Boehringer Ingelheim Investigational Site
Jaipur, Rajasthan
1160.71.1067 Boehringer Ingelheim Investigational Site
Kerala
1160.71.1068 Boehringer Ingelheim Investigational Site
Kottayam
1160.71.1055 Boehringer Ingelheim Investigational Site
Lucknow, Uttar Pradesh
1160.71.1051 Boehringer Ingelheim Investigational Site
Ludhiana
1160.71.1072 Boehringer Ingelheim Investigational Site
Mysore
1160.71.1059 Boehringer Ingelheim Investigational Site
Nagpur-12
1160.71.1052 Boehringer Ingelheim Investigational Site
New Delhi
1160.71.1070 Boehringer Ingelheim Investigational Site
Pune, Maharashtra
Taiwan13 sites
1160.71.1680 Boehringer Ingelheim Investigational Site
Changhua
1160.71.1683 Boehringer Ingelheim Investigational Site
Hualien City
1160.71.1682 Boehringer Ingelheim Investigational Site
Kaohsiung City
1160.71.1679 Boehringer Ingelheim Investigational Site
Taichung
1160.71.1681 Boehringer Ingelheim Investigational Site
Tainan
1160.71.1671 Boehringer Ingelheim Investigational Site
Taipei
1160.71.1672 Boehringer Ingelheim Investigational Site
Taipei
1160.71.1673 Boehringer Ingelheim Investigational Site
Taipei
1160.71.1674 Boehringer Ingelheim Investigational Site
Taipei
1160.71.1675 Boehringer Ingelheim Investigational Site
Taipei
1160.71.1676 Boehringer Ingelheim Investigational Site
Taipei
1160.71.1677 Boehringer Ingelheim Investigational Site
Taipei
1160.71.1678 Boehringer Ingelheim Investigational Site
Taoyuan
Russia12 sites
1160.71.1501 Boehringer Ingelheim Investigational Site
Moscow
1160.71.1503 Boehringer Ingelheim Investigational Site
Moscow
1160.71.1504 Boehringer Ingelheim Investigational Site
Moscow
1160.71.1505 Boehringer Ingelheim Investigational Site
Moscow
1160.71.1507 Boehringer Ingelheim Investigational Site
Moscow
1160.71.1508 Boehringer Ingelheim Investigational Site
Moscow
1160.71.1509 Boehringer Ingelheim Investigational Site
Moscow
1160.71.1510 Boehringer Ingelheim Investigational Site
Moscow
1160.71.1511 Boehringer Ingelheim Investigational Site
Moscow
1160.71.1512 Boehringer Ingelheim Investigational Site
Saint Petersburg
1160.71.1513 Boehringer Ingelheim Investigational Site
Saint Petersburg
1160.71.1514 Boehringer Ingelheim Investigational Site
Saint Petersburg
China11 sites
1160.71.0771 Boehringer Ingelheim Investigational Site
Beijing
1160.71.0772 Boehringer Ingelheim Investigational Site
Beijing
1160.71.0773 Boehringer Ingelheim Investigational Site
Beijing
1160.71.0774 Boehringer Ingelheim Investigational Site
Beijing
1160.71.0776 Boehringer Ingelheim Investigational Site
Haerbin
1160.71.0784 Boehringer Ingelheim Investigational Site
Hangzhou
1160.71.0778 Boehringer Ingelheim Investigational Site
Qingdao
1160.71.0781 Boehringer Ingelheim Investigational Site
Shanghai
1160.71.0782 Boehringer Ingelheim Investigational Site
Shanghai
1160.71.0777 Boehringer Ingelheim Investigational Site
Shenyang
1160.71.0780 Boehringer Ingelheim Investigational Site
Shijiazhuang
Denmark11 sites
1160.71.0837 Boehringer Ingelheim Investigational Site
Aalborg
1160.71.0835 Boehringer Ingelheim Investigational Site
Aarhus C
1160.71.0833 Boehringer Ingelheim Investigational Site
Elsinore
1160.71.0838 Boehringer Ingelheim Investigational Site
Frederikssund
1160.71.0834 Boehringer Ingelheim Investigational Site
Herlev
1160.71.0841 Boehringer Ingelheim Investigational Site
Horsens
1160.71.0832 Boehringer Ingelheim Investigational Site
Hvidovre
1160.71.0840 Boehringer Ingelheim Investigational Site
Køge
1160.71.0831 Boehringer Ingelheim Investigational Site
Odense
1160.71.0839 Boehringer Ingelheim Investigational Site
Roskilde
1160.71.0836 Boehringer Ingelheim Investigational Site
Svendborg
South Korea11 sites
1160.71.1585 Boehringer Ingelheim Investigational Site
Busan
1160.71.1586 Boehringer Ingelheim Investigational Site
Cheonan-si
1160.71.1584 Boehringer Ingelheim Investigational Site
Daegu
1160.71.1591 Boehringer Ingelheim Investigational Site
Daegu
1160.71.1590 Boehringer Ingelheim Investigational Site
Gwangju
1160.71.1581 Boehringer Ingelheim Investigational Site
Incheon
1160.71.1582 Boehringer Ingelheim Investigational Site
Seoul
1160.71.1583 Boehringer Ingelheim Investigational Site
Seoul
1160.71.1589 Boehringer Ingelheim Investigational Site
Seoul
1160.71.1592 Boehringer Ingelheim Investigational Site
Seoul
1160.71.1593 Boehringer Ingelheim Investigational Site
Seoul
Sweden11 sites
1160.71.1633 Boehringer Ingelheim Investigational Site
Gothenburg
1160.71.1627 Boehringer Ingelheim Investigational Site
Malmö
1160.71.1628 Boehringer Ingelheim Investigational Site
Nässjö
1160.71.1625 Boehringer Ingelheim Investigational Site
Norrköping
1160.71.1623 Boehringer Ingelheim Investigational Site
Örebro
1160.71.1626 Boehringer Ingelheim Investigational Site
Stockholm
1160.71.1634 Boehringer Ingelheim Investigational Site
Stockholm
1160.71.1624 Boehringer Ingelheim Investigational Site
Umeå
1160.71.1621 Boehringer Ingelheim Investigational Site
Uppsala
1160.71.1635 Boehringer Ingelheim Investigational Site
Uppsala
1160.71.1622 Boehringer Ingelheim Investigational Site
Västerås
United Kingdom10 sites
1160.71.1744 Boehringer Ingelheim Investigational Site
Birmingham
1160.71.1746 Boehringer Ingelheim Investigational Site
Chertsey
1160.71.1745 Boehringer Ingelheim Investigational Site
County Armagh
1160.71.1755 Boehringer Ingelheim Investigational Site
Kirkcaldy, Fife
1160.71.1741 Boehringer Ingelheim Investigational Site
London
1160.71.1742 Boehringer Ingelheim Investigational Site
Newcastle upon Tyne
1160.71.1751 Boehringer Ingelheim Investigational Site
Newport
1160.71.1752 Boehringer Ingelheim Investigational Site
Northampton
1160.71.1743 Boehringer Ingelheim Investigational Site
Romford, Essex
1160.71.1748 Boehringer Ingelheim Investigational Site
York
Czechia9 sites
1160.71.0816 Boehringer Ingelheim Investigational Site
Modřice
1160.71.0820 Boehringer Ingelheim Investigational Site
Ostrava
1160.71.0818 Boehringer Ingelheim Investigational Site
Pardubice
1160.71.0814 Boehringer Ingelheim Investigational Site
Plzen-Bory
1160.71.0811 Boehringer Ingelheim Investigational Site
Prague
1160.71.0812 Boehringer Ingelheim Investigational Site
Prague
1160.71.0813 Boehringer Ingelheim Investigational Site
Prague
1160.71.0817 Boehringer Ingelheim Investigational Site
Příbram
1160.71.0819 Boehringer Ingelheim Investigational Site
Ústí nad Orlicí
Hungary9 sites
1160.71.1011 Boehringer Ingelheim Investigational Site
Budapest
1160.71.1012 Boehringer Ingelheim Investigational Site
Budapest
1160.71.1013 Boehringer Ingelheim Investigational Site
Budapest
1160.71.1014 Boehringer Ingelheim Investigational Site
Budapest
1160.71.1015 Boehringer Ingelheim Investigational Site
Budapest
1160.71.1016 Boehringer Ingelheim Investigational Site
Budapest
1160.71.1020 Boehringer Ingelheim Investigational Site
Gyöngyös
1160.71.1017 Boehringer Ingelheim Investigational Site
Komárom
1160.71.1018 Boehringer Ingelheim Investigational Site
Pécs
Austria8 sites
1160.71.0543 Boehringer Ingelheim Investigational Site
Graz
1160.71.0549 Boehringer Ingelheim Investigational Site
Linz
1160.71.0541 Boehringer Ingelheim Investigational Site
Vienna
1160.71.0542 Boehringer Ingelheim Investigational Site
Vienna
1160.71.0545 Boehringer Ingelheim Investigational Site
Vienna
1160.71.0547 Boehringer Ingelheim Investigational Site
Vienna
1160.71.0548 Boehringer Ingelheim Investigational Site
Vienna
1160.71.0550 Boehringer Ingelheim Investigational Site
Wiener Neustadt
Australia7 sites
1160.71.0509 Boehringer Ingelheim Investigational Site
Ashford, South Australia
1160.71.0504 Boehringer Ingelheim Investigational Site
Box Hill, Victoria
1160.71.0508 Boehringer Ingelheim Investigational Site
Coffs Harbour, New South Wales
1160.71.0501 Boehringer Ingelheim Investigational Site
Geelong, Victoria
1160.71.0510 Boehringer Ingelheim Investigational Site
Gosford, New South Wales
1160.71.0507 Boehringer Ingelheim Investigational Site
Launceston, Tasmania
1160.71.0506 Boehringer Ingelheim Investigational Site
Milton, Queensland
Brazil7 sites
1160.71.0644 Boehringer Ingelheim Investigational Site
Campinas
1160.71.0650 Boehringer Ingelheim Investigational Site
Curitiba
1160.71.0651 Boehringer Ingelheim Investigational Site
Curitiba
1160.71.0652 Boehringer Ingelheim Investigational Site
Goiânia
1160.71.0646 Boehringer Ingelheim Investigational Site
Sao Jose Do Riio Preto
1160.71.0647 Boehringer Ingelheim Investigational Site
São José do Rio Preto
1160.71.0643 Boehringer Ingelheim Investigational Site
São Paulo
Bulgaria7 sites
1160.71.0620 Boehringer Ingelheim Investigational Site
Pleven
1160.71.0611 Boehringer Ingelheim Investigational Site
Sofia
1160.71.0612 Boehringer Ingelheim Investigational Site
Sofia
1160.71.0615 Boehringer Ingelheim Investigational Site
Sofia
1160.71.0617 Boehringer Ingelheim Investigational Site
Sofia
1160.71.0618 Boehringer Ingelheim Investigational Site
Sofia
1160.71.0625 Boehringer Ingelheim Investigational Site
Sofia
Poland7 sites
1160.71.1436 Boehringer Ingelheim Investigational Site
Gdynia
1160.71.1437 Boehringer Ingelheim Investigational Site
Gdynia
1160.71.1438 Boehringer Ingelheim Investigational Site
Gdynia
1160.71.1433 Boehringer Ingelheim Investigational Site
Puławy
1160.71.1431 Boehringer Ingelheim Investigational Site
Warsaw
1160.71.1432 Boehringer Ingelheim Investigational Site
Warsaw
1160.71.1434 Boehringer Ingelheim Investigational Site
Zabrze
Finland6 sites
1160.71.0851 Boehringer Ingelheim Investigational Site
Helsinki
1160.71.0859 Boehringer Ingelheim Investigational Site
Jyväskylä
1160.71.0854 Boehringer Ingelheim Investigational Site
Oulu
1160.71.0858 Boehringer Ingelheim Investigational Site
Pori
1160.71.0852 Boehringer Ingelheim Investigational Site
Tampere
1160.71.0853 Boehringer Ingelheim Investigational Site
Turku
Greece6 sites
1160.71.0901 Boehringer Ingelheim Investigational Site
Athens
1160.71.0914 Boehringer Ingelheim Investigational Site
Kalamaria-Thessaloniki
1160.71.0904 Boehringer Ingelheim Investigational Site
Larissa
1160.71.0910 Boehringer Ingelheim Investigational Site
Thebes
1160.71.0903 Boehringer Ingelheim Investigational Site
Trikala
1160.71.0905 Boehringer Ingelheim Investigational Site
Voula - Athens
Norway6 sites
1160.71.1396 Boehringer Ingelheim Investigational Site
Gjøvik
1160.71.1393 Boehringer Ingelheim Investigational Site
Moss
1160.71.1395 Boehringer Ingelheim Investigational Site
Nordbyhagen
1160.71.1391 Boehringer Ingelheim Investigational Site
Oslo
1160.71.1397 Boehringer Ingelheim Investigational Site
Oslo
1160.71.1394 Boehringer Ingelheim Investigational Site
Rud
Portugal6 sites
1160.71.1456 Boehringer Ingelheim Investigational Site
Amadora
1160.71.1451 Boehringer Ingelheim Investigational Site
Carnaxide
1160.71.1454 Boehringer Ingelheim Investigational Site
Coimbra
1160.71.1459 Boehringer Ingelheim Investigational Site
Coimbra
1160.71.1457 Boehringer Ingelheim Investigational Site
Covilha
1160.71.1455 Boehringer Ingelheim Investigational Site
Porto
Slovakia6 sites
1160.71.1548 Boehringer Ingelheim Investigational Site
Banská Bystrica
1160.71.1541 Boehringer Ingelheim Investigational Site
Bratislava
1160.71.1542 Boehringer Ingelheim Investigational Site
Bratislava
1160.71.1543 Boehringer Ingelheim Investigational Site
Bratislava
1160.71.1550 Boehringer Ingelheim Investigational Site
Košice
1160.71.1547 Boehringer Ingelheim Investigational Site
Žilina
Philippines5 sites
1160.71.1422 Boehringer Ingelheim Investigational Site
Ermita Manila
1160.71.1421 Boehringer Ingelheim Investigational Site
Manila
1160.71.1424 Boehringer Ingelheim Investigational Site
Pasig
1160.71.1423 Boehringer Ingelheim Investigational Site
Quezon City
1160.71.1425 Boehringer Ingelheim Investigational Site
Quezon City
Switzerland4 sites
1160.71.1652 Boehringer Ingelheim Investigational Site
Basel
1160.71.1655 Boehringer Ingelheim Investigational Site
Bellinzona
1160.71.1651 Boehringer Ingelheim Investigational Site
Bern
1160.71.1654 Boehringer Ingelheim Investigational Site
Lugano
Italy3 sites
1160.71.1169 Boehringer Ingelheim Investigational Site
Arezzo
1160.71.1172 Boehringer Ingelheim Investigational Site
Ascoli Piceno
1160.71.1170 Boehringer Ingelheim Investigational Site
Sassari
Thailand3 sites
1160.71.1701 Boehringer Ingelheim Investigational Site
Bangkok
1160.71.1703 Boehringer Ingelheim Investigational Site
Chiang Mai
1160.71.1704 Boehringer Ingelheim Investigational Site
Khon Kaen
Hong Kong2 sites
1160.71.1003 Boehringer Ingelheim Investigational Site
Kowloon
1160.71.1004 Boehringer Ingelheim Investigational Site
Kowloon
Malaysia2 sites
1160.71.1291 Boehringer Ingelheim Investigational Site
Kuala Lumpur
1160.71.1292 Boehringer Ingelheim Investigational Site
Kuala Lumpur
Romania2 sites
1160.71.1471 Boehringer Ingelheim Investigational Site
Bucharest
1160.71.1472 Boehringer Ingelheim Investigational Site
Bucharest
Singapore1 site
1160.71.1531 Boehringer Ingelheim Investigational Site
Singapore
About this study
Official title: RELY-ABLE Long Term Multi-center Extension of Dabigatran Treatment in Patients With Atrial Fibrillation Who Completed the RE-LY Trial and a Cluster Randomised Trial to Assess the Effect of a Knowledge Translation Intervention on Patient Outcomes
The purposes of this study are:
- To evaluate the long-term safety of dabigatran etexilate
- To assess the effect of a knowledge translation intervention on patient outcomes
- Conditions
- Atrial Fibrillation
- Being tested
- dabigatran dose 1, dabigatran dose 2
- Medical subject headings
- Atrial Fibrillation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
dabigatran dose 1Drug
dabigatran high dose twice daily
dabigatran dose 2Drug
dabigatran low dose twice daily
| Study group | Role | What they receive |
|---|---|---|
| dabigatran dose 1 | Experimental | dabigatran high dose twice daily Receives: Drug: dabigatran dose 1 |
| dabigatran dose 2 | Experimental | dabigatran low dose twice daily Receives: Drug: dabigatran dose 2 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Major Bleeding, Annualized Rate of Subjects With Major Bleeds
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Major bleeding must have satisfied one or more of the following criteria:
- Bleeding associated with a reduction in hemoglobin of at least 20 g/L
- Required transfusion of at least 2 units of blood or packed cells
- Symptomatic bleeding in a critical area or organ: intraocular, intraspinal, intramuscular with compartment syndrome, retroperitoneal, intra-articular, pericardial, gastrointestinal
Major bleed were classified as life-threatening if they met one or more of the following criteria:
- Reduction in hemoglobin of at least 50 g/L
- Transfusion of at least 4 units of blood or packed cells
- Symptomatic intracranial bleeding, either subdural or intracerebral
- Associated with hypotension requiring use of intravenous inotropic agents
- Required surgical intervention to stop bleeding
- Resulted in death
Measured: up to 43 months
Secondary outcomes (13)
Stroke, Annualized Rate of Subjects With Stroke
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Stroke was an acute onset of a focal neurological deficit of presumed vascular origin lasting for 24 hours or more or resulting in death. The stroke was categorized as ischemic or hemorrhagic or cause unknown based on computerized tomography (CT), magnetic resonance (MR) scanning or autopsy. Fatal stroke was defined as death from any cause within 30 days of stroke. Severity of stroke was assessed by modified Rankin score at discharge from hospital
Measured: up to 43 months
Non CNS Systemic Embolism (SEE), Annualized Rate of Subjects With Non-CNS SEE
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Systemic embolism was an acute vascular occlusion of the extremities or any organ (kidneys, mesenteric arteries, spleen, retina or grafts), and was to be documented by angiography, surgery, scintigraphy, or autopsy.
Measured: up to 43 months
Pulmonary Embolism (PE), Annualized Rate of Subjects With PE
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Pulmonary Embolism was generally documented by one of the following:
- an intraluminal filling defect in segmental or more proximal branches on spiral CT scan
- an intraluminal filling defect or an extension of an existing defect or a sudden cutoff of vessels more than 2.5 mm in diameter on the pulmonary angiogram
- a perfusion defect of at least 75% of a segment with a local normal ventilation result (high-probability) on ventilation/perfusion lung scan (VPLS)
- inconclusive spiral CT, pulmonary angiography or lung scintigraphy with demonstration of DVT in the lower extremities by compression ultrasound or venography.
Measured: up to 43 months
Acute Myocardial Infarction (MI), Annualized Rate of Subjects With MI
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
- In subjects not undergoing PCI or CABG a subject should have fulfilled at least 2 of the following: i. Typical prolonged severe chest pain or related symptoms or signs suggestive of MI. ii. Elevation of troponin or CK-MB to more than upper level of normal (ULN) or, if CK-MB was elevated at baseline, re-elevation to more than 50% increase above the previous level. iii. Development of significant Q-waves in at least 2 adjacent ECG leads. b. After percutaneous coronary intervention (within 24h). c. After coronary artery bypass grafting (within 72h). d. Silent myocardial infarction. e. Myocardial infarction could also have been demonstrated at autopsy.
Measured: up to 43 months
Deep Vein Thrombosis, Annualized Rate of Subjects With DVT
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Deep Vein Thrombosis (DVT) was generally documented by one of the following:
- abnormal compression ultrasound (CUS),
- an intraluminal filling defect on venography.
Measured: up to 43 months
Death, Annualized Rate of Subject Death
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Deaths were classified as being vascular (sudden/arrhythmic, pump failure death, or other vascular, including bleeding) or non-vascular, due to other specified causes (e.g., malignancy), or of unknown etiology.
Measured: up to 43 months
Annualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE)
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Measured: up to 43 months
Annualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE) and All Cause Death
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Measured: up to 43 months
Annualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE), Pulmonary Embolism (PE), Myocardial Infarction, Vascular Death
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Measured: up to 43 months
Annualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE), Pulmonary Embolism (PE), Myocardial Infarction (MI), All Cause Death and Major Bleed
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Measured: up to 43 months
Annualized Rate of Subjects With Minor Bleeds
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Minor bleeds were clinical bleeds that did not fulfill the criteria for major bleeds. Minor bleeds were classified as associated with study medication discontinuation (temporary or permanent) or not.
Measured: up to 43 months
Annualized Rate of Subjects With Any Bleeds (Major Plus Minor)
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Measured: up to 43 months
Annualized Rate of Subjects With Intra-Cranial Hemorrhage (ICH)
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25.
Measured: up to 43 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Dec 2008 (estimated)
- Study startNov 2008
- Primary completionDec 2012
- Study completionDec 2012
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Atrial FibrillationStudies of the same condition, open and under way.
- More trials run by Boehringer IngelheimThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Enrolment
- 5,897 participants (actual)
Sponsor and investigators
- Lead sponsor
- Boehringer Ingelheim
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Boehringer Ingelheim, Study chair, Boehringer Ingelheim
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00808067
- Sponsor's protocol ID
- 1160.71
- Other IDs
- 2008-005248-17, 2008
- Status last verified
- Mar 2014
- First submitted
- 12 Dec 2008
- Last updated
- 9 Jun 2014
- Results posted
- Yes, on ClinicalTrials.gov
Publications
Connolly SJ, Wallentin L, Ezekowitz MD, Eikelboom J, Oldgren J, Reilly PA, Brueckmann M, Pogue J, Alings M, Amerena JV, Avezum A, Baumgartner I, Budaj AJ, Chen JH, Dans AL, Darius H, Di Pasquale G, Ferreira J, Flaker GC, Flather MD, Franzosi MG, Golitsyn SP, Halon DA, Heidbuchel H, Hohnloser SH, Huber K, Jansky P, Kamensky G, Keltai M, Kim SS, Lau CP, Le Heuzey JY, Lewis BS, Liu L, Nanas J, Omar R, Pais P, Pedersen KE, Piegas LS, Raev D, Smith PJ, Talajic M, Tan RS, Tanomsup S, Toivonen L, Vinereanu D, Xavier D, Zhu J, Wang SQ, Duffy CO, Themeles E, Yusuf S. The Long-Term Multicenter Observational Study of Dabigatran Treatment in Patients With Atrial Fibrillation (RELY-ABLE) Study. Circulation. 2013 Jul 16;128(3):237-43. doi: 10.1161/CIRCULATIONAHA.112.001139. Epub 2013 Jun 14.
PubMed 23770747
Study at a glance
From the registry record, last updated by the sponsor on 9 Jun 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- RELY-ABLE Long Term Multi-center Extension of Dabigatran Treatment in Patients With Atrial Fibrillation Who Completed the RE-LY Trial and a Cluster Randomised Trial to Assess the Effect of a Knowledge Translation Intervention on Patient Outcomes
- ClinicalTrials.gov ID
- NCT00808067
- Acronym / sponsor ID
- 1160.71
- Conditions
- Atrial Fibrillation
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 5,897 participants (actual)
- Lead sponsor
- Boehringer IngelheimIndustry (pharma, biotech, devices)
- Study start
- Nov 2008
- Primary completion
- Dec 2012 (actual)
- Study completion
- Dec 2012 (actual)
- First posted
- 15 Dec 2008 (estimated)
- Results
- Posted 8 Apr 2014
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purposes of this study are:
- To evaluate the long-term safety of dabigatran etexilate
- To assess the effect of a knowledge translation intervention on patient outcomes
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| dabigatran dose 1 | Experimental | Drug: dabigatran dose 1dabigatran high dose twice daily |
| dabigatran dose 2 | Experimental | Drug: dabigatran dose 2dabigatran low dose twice daily |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Participation in RE-LY, requires long term anticoagulation, provides written informed consent
Key exclusion criteria (1 listed)
- Permanent discontinuation of dabigatran during RE-LY
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| dabigatran dose 1dabigatran high dose twice daily | Drug | dabigatran dose 1 |
| dabigatran dose 2dabigatran low dose twice daily | Drug | dabigatran dose 2 |
Primary outcome
Major Bleeding, Annualized Rate of Subjects With Major Bleeds
Time frame: up to 43 months
Annualized event rate (%) = 100 * No. subjects with event / subject-years. Subject-years = Sum (date of last visit - date of first dose + 1) of all subjects / 365.25. Major bleeding must have satisfied one or more of the following criteria: * Bleeding associated with a reduction in hemoglobin of at least 20 g/L * Required transfusion of at least 2 units of blood or packed cells * Symptomatic bleeding in a critical area or organ: intraocular, intraspinal, intramuscular with compartment syndrome, retroperitoneal, intra-articular, pericardial, gastrointestinal Major bleed were classified as life-threatening if they met one or more of the following criteria: * Reduction in hemoglobin of at least 50 g/L * Transfusion of at least 4 units of blood or packed cells * Symptomatic intracranial bleeding, either subdural or intracerebral * Associated with hypotension requiring use of intravenous inotropic agents * Required surgical intervention to stop bleeding * Resulted in death
13 secondary outcomes
Stroke, Annualized Rate of Subjects With Stroke
Time frame: up to 43 months
Non CNS Systemic Embolism (SEE), Annualized Rate of Subjects With Non-CNS SEE
Time frame: up to 43 months
Pulmonary Embolism (PE), Annualized Rate of Subjects With PE
Time frame: up to 43 months
Acute Myocardial Infarction (MI), Annualized Rate of Subjects With MI
Time frame: up to 43 months
Deep Vein Thrombosis, Annualized Rate of Subjects With DVT
Time frame: up to 43 months
Death, Annualized Rate of Subject Death
Time frame: up to 43 months
Annualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE)
Time frame: up to 43 months
Annualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE) and All Cause Death
Time frame: up to 43 months
Annualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE), Pulmonary Embolism (PE), Myocardial Infarction, Vascular Death
Time frame: up to 43 months
Annualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE), Pulmonary Embolism (PE), Myocardial Infarction (MI), All Cause Death and Major Bleed
Time frame: up to 43 months
Annualized Rate of Subjects With Minor Bleeds
Time frame: up to 43 months
Annualized Rate of Subjects With Any Bleeds (Major Plus Minor)
Time frame: up to 43 months
Annualized Rate of Subjects With Intra-Cranial Hemorrhage (ICH)
Time frame: up to 43 months
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Jun 2014.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 23770747Connolly SJ, Wallentin L, Ezekowitz MD, Eikelboom J, Oldgren J, Reilly PA, Brueckmann M, Pogue J, Alings M, Amerena JV, Avezum A, Baumgartner I, Budaj AJ, Chen JH, Dans AL, Darius H, Di Pasquale G, Ferreira J, Flaker GC, Flather MD, Franzosi MG, Golitsyn SP, Halon DA, Heidbuchel H, Hohnloser SH, Huber K, Jansky P, Kamensky G, Keltai M, Kim SS, Lau CP, Le Heuzey JY, Lewis BS, Liu L, Nanas J, Omar R, Pais P, Pedersen KE, Piegas LS, Raev D, Smith PJ, Talajic M, Tan RS, Tanomsup S, Toivonen L, Vinereanu D, Xavier D, Zhu J, Wang SQ, Duffy CO, Themeles E, Yusuf S. The Long-Term Multicenter Observational Study of Dabigatran Treatment in Patients With Atrial Fibrillation (RELY-ABLE) Study. Circulation. 2013 Jul 16;128(3):237-43. doi: 10.1161/CIRCULATIONAHA.112.001139. Epub 2013 Jun 14.
- Related InfoLink provided by the sponsor.
- Related InfoLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Boehringer Ingelheim study chair
Boehringer Ingelheim
567 sites in 35 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing dabigatran dose 1 and dabigatran dose 2 in people with Atrial Fibrillation, run by Boehringer Ingelheim at 567 sites in 35 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 9 Jun 2014. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 567 sites in United States, Canada, Netherlands, France, Israel and 30 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 8 Apr 2014). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Major Bleeding, Annualized Rate of Subjects With Major Bleeds (time frame: up to 43 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00808067, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jun 2014.