InsomniaPhase 4NCT00386334
A Long-Term Safety and Efficacy Study of Eszopiclone in Elderly With Primary Chronic Insomnia
A Phase 4 study testing Eszopiclone in people with Insomnia, run by Sumitomo Pharma America, Inc. at 82 sites in United States.
Trial summary
To evaluate the long-term safety and efficacy of eszopiclone administered for 12 weeks in elderly subjects with primary chronic insomnia.Administration of eszopiclone 2 mg daily at bedtime for 12 weeks in elderly subjects with a diagnosis of primary chronic insomnia will be safe and well tolerated, improve subjective… Read more about this study
- Who is it for?
- Ages 65 to 85 years
- Conditions the study is for
- Insomnia
- What is being tested?
- Eszopiclone
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 388 participants
- Where
- 82 sitesUnited States
- Study dates
- Oct 2006to Feb 2008
- Phase
- Phase 4
- 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 65 to 85 years
- All sexes
- No healthy volunteers
- Older adult
Who may be able to join
- Male and female subjects with primary chronic insomnia. Subject is otherwise in good general health, based on screening physical examination and medical history.
Who cannot join
- Subject has recent history of known clinically significant abnormal laboratory findings.
Trial locations and contacts
82 sites in 1 country.
82 sites in 1 country
United States82 sites
Study site
Albuquerque, New Mexico, 87106
Study site
Allentown, Pennsylvania, 18104
Study site
Anaheim, California, 92801
Anderson Pharmaceutical Research
Anderson, South Carolina, 29521
Study site
Anderson, South Carolina, 29621
Study site
Atlanta, Florida, 30342
Study site
Baltimore, Maryland, 21208
Study site
Baton Rouge, Louisiana, 70809
Study site
Beachwood, Ohio, 44122
Study site
Birmingham, Alabama, 35226
Study site
Boston, Massachusetts, 02135
Study site
Braintree, Massachusetts, 02184
Study site
Brooklyn, New York, 11235
Study site
Cary, North Carolina, 27540
Study site
Chandler, Arizona, 85225
Study site
Chicago, Illinois, 60610
Study site
Chicago, Illinois, 60634
Study site
Cincinnati, Ohio, 45206
Study site
Clearwater, Florida, 33765
Study site
Cleveland, Ohio, 44122
Study site
Colorado Springs, Colorado, 80918
Study site
Coral Springs, Florida, 33065
Study site
Crestview Hills, Kentucky, 41017
Study site
Dallas, Texas, 75231
Study site
Dayton, Ohio, 45408
Study site
Delray Beach, Florida, 33458
Study site
Denver, Colorado, 80212
Study site
Duncansville, Pennsylvania, 16635
Study site
Durham, North Carolina, 27710
Study site
Evansville, Indiana, 47714
Study site
Fairfax, Virginia, 22030
Study site
Florissant, Missouri, 63031
Study site
Fort Myers, Florida, 33912
Study site
Gables, Florida, 33134
Study site
Glendale, Arizona, 85306
Study site
Hamilton, New Jersey, 08690
Study site
Hickory, North Carolina, 28601
Study site
Honolulu, Hawaii, 96814
Study site
Houston, Texas, 77024
Study site
Irvine, California, 92618
Study site
Jupiter, Florida, 33458
Study site
La Mesa, California, 91942
Study site
Lexington, Kentucky, 40509
Study site
Los Angeles, California, 90024
Study site
Maitland, Florida, 32751
Study site
Mineola, New York, 11501
Study site
Mogadore, Ohio, 44260
Study site
Naples, Florida, 34110
Study site
New Bern, North Carolina, 28562
Study site
New York, New York, 10021
Study site
New York, New York, 10023
Study site
Newton, Massachusetts, 02459
Study site
Oklahoma City, Oklahoma, 73103
Study site
Oklahoma City, Oklahoma, 73112
Study site
Oklahoma City, Oklahoma, 73118
Study site
Orlando, Florida, 32806
Study site
Overland Park, Kansas, 66212
Study site
Pembroke Pines, Florida, 33024
Study site
Pinellas Park, Florida, 33781
Study site
Prairie Village, Kansas, 66206
Study site
Richmond, Virginia, 23229
Study site
Rochester, New York, 14609
Study site
San Antonio, Texas, 78205
Study site
San Antonio, Texas, 78229
Study site
San Antonio, Texas, 78238
Study site
San Diego, California, 92108
Study site
San Diego, California, 92121
Study site
San Diego, California, 92123
Study site
Sarasota, Florida, 34238
Study site
Scotland, Pennsylvania, 17254
Study site
Simpsonville, South Carolina, 29681
Study site
Spokane, Washington, 99204
Study site
St. Petersburg, Florida, 33707
Study site
St. Petersburg, Florida, 33709
Study site
Stockbridge, Georgia, 30281
Study site
Tucson, Arizona, 85712
Study site
Vernon Hills, Illinois, 60061
Study site
Vero Beach, Florida, 32960
Study site
Warwick, Rhode Island, 02886
Study site
West Palm Beach, Florida, 33407
Study site
Wichita Falls, Texas, 76309
Study site
Winston-Salem, North Carolina, 27157
About this study
Official title: A Long-Term Safety and Efficacy Study of Eszopiclone in Elderly Subjects With Primary Chronic Insomnia
To evaluate the long-term safety and efficacy of eszopiclone administered for 12 weeks in elderly subjects with primary chronic insomnia.Administration of eszopiclone 2 mg daily at bedtime for 12 weeks in elderly subjects with a diagnosis of primary chronic insomnia will be safe and well tolerated, improve subjective sleep measures, improve measures of Quality of Life and next day insomnia symptoms, and have no significant withdrawal central nervous system adverse events or rebound insomnia.
Read the detailed description
A double-blind, randomized, placebo controlled, parallel group study of eszopiclone in elderly subjects with primary chronic insomnia. The study will involve up to 9 visits and subject participation will be approximately 18 weeks. This study was previously posted by Sepracor Inc. In October 2009, Sepracor Inc. was acquired by Dainippon Sumitomo Pharma., and in October 2010, Sepracor Inc's name was changed to Sunovion Pharmaceuticals Inc.
- Conditions
- Insomnia
- Being tested
- Eszopiclone, Placebo
- Keywords
- insomnia, chronic, primary
- Medical subject headings
- Sleep Initiation and Maintenance Disorders, Bronchiolitis Obliterans Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
EszopicloneDrug
Also called Lunesta
2 mg tablet once per day in the evening
PlaceboDrug
Tablet one per day in the evening.
| Study group | Role | What they receive |
|---|---|---|
| Placebo | Placebo comparator | Week -2 to day 0 single blind one tablet placebo in the evening. Double blind period: Day 1 to Week 12 double blind one tablet placebo in the evening. Follow up period: two weeks (Weeks 13-14) single blind one tablet placebo in evening, and two weeks (Weeks 15-16) no drug washout. Receives: Drug: Placebo |
| Eszopiclone | Experimental | Week -2 to day 0 single blind one tablet placebo in evening. Double Blind period: Day 1 to Week 12 double blind one tablet 2 mg of eszopiclone in evening. Follow up period consists of two weeks (Weeks 13-14) single blind one tablet placebo in evening, and two weeks (Weeks 15-16) no drug washout. Receives: Drug: Eszopiclone; Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Mean Change From Baseline in Subject-Reported Total Sleep Time (TST) Averaged Over the 12 Week Double Blind Study Period.
The difference between the total sleep time at baseline and the average total sleep time over the double blind period(average of post-dose values from weeks 3,6,9,12) reported by the participant. The change is calculated as the average over the double blind period minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose)-12 weeks
Secondary outcomes (68)
Mean Change From Baseline in Subject-reported Total Sleep Time at Various Study Time Points.
The difference between the total sleep time at baseline and at different time points in the double-blind period (weeks 3,6,9,12), the single-blind follow-up (week 14) and the non-drug treatment follow-up (week 16). The change is calculated as the time point value minus the baseline value.
Measured: Weeks 0, 3, 6, 9, 12, 14, 16
Mean Subject-reported Total Sleep Time in Minutes at Various Study Time Points.
The mean total minutes asleep each night at different time points: baseline(week 0), double-blind phase(weeks 3,6,9,12), the single-blind follow-up(week 14),the non-drug treatment follow-up(week 16), and the double-blind average(average of weeks 3,6,9,12 values).
Measured: Weeks 0, 3, 6, 9, 12, 14, 16
Mean Change From Baseline in Subject-reported Sleep Latency (SL) Averaged Over the 12 Week Double Blind Period.
Sleep latency answers how long it takes to fall asleep. The difference between the sleep latency at baseline and the average sleep latency over the double blind period(average of post-dose values from weeks 3,6,9,12) reported by the participant. The change is calculated as the average over the double blind period minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - Week12
Mean Change From Baseline in Subject-reported Sleep Latency at Various Study Time Points
Sleep latency answers the question: How long did it take you to fall asleep last night? The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Sleep Latency Reported at Various Study Time Points.
Sleep latency answers the question: How long did it take you to fall asleep last night? Mean values are reported at baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), and the average for the entire double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Wake Time After Sleep Onset (WASO) Averaged Over the 12 Week Double-blind Study Period.
Wake time after sleep onset (WASO) is the time spent awake from sleep onset to final awakening. The difference between WASO at baseline and the average WASO over the double blind period(average of post-dose values from weeks 3,6,9,12). The change is calculated as the average over the double blind period minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) -week 12
Mean Change From Baseline in Subject-reported Wake Time After Sleep Onset (WASO) at Various Study Time Points.
Wake time after sleep onset is the time spent awake from sleep onset to final awakening. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), weeks 3,6,9,12,14,16
Mean Subject-reported Wake Time After Sleep Onset (WASO) at Various Study Time Points
Wake time after sleep onset is the time spent awake from sleep onset to final awakening. Mean values are reported at baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), and the average for the entire double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Number of Awakenings Averaged Over the 12 Week Double Blind Study Period.
The number of awakenings is the number of times a subject wakes up between the initial onset of sleep and the final awakening. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - Week12
Mean Change From Baseline in the Number of Subject-reported Awakenings at Various Study Time Points.
The number of awakenings refers to the number of times a subject wakes up between the initial onset of sleep and the final awakening. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Number of Awakenings (Subject-reported) at Various Study Time Points
Number of awakenings is number of times a subject wakes up between initial onset of sleep and final awakening. Mean values are reported at baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), and the average for the double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Quality of Sleep Averaged Over the 12 Week Double Blind Study Period
Quality of sleep was rated by participants on a scale of 0-10, with higher scores representing better quality sleep. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - Week12
Mean Change From Baseline in Subject-reported Quality of Sleep at Various Study Time Points.
Sleep quality was rated by subjects on a scale from 0-10, with higher scores representing better quality sleep. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Ratings of Subject-reported Quality of Sleep at Various Study Time Points
Quality of sleep was rated by participants on a scale of 0-10, with higher scores representing better quality sleep. Mean values are reported at baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), and the average for the double-blind phase(average of weeks 3,6,9,12 values).
Measured: weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-Reported Depth of Sleep for the Average Reported During the Double-blind Period.
Depth of sleep was reported by study participants using a scale from 0-10, with higher scores representing better sleep. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Depth of Sleep at Various Study Time Points
Depth of sleep was reported by study participants using a scale from 0-10, with higher scores representing better sleep. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Depth of Sleep at Various Study Time Points
Depth of sleep was reported by study participants using a scale from 0-10, with higher scores representing better sleep. Mean values reported: baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), and the average for the double-blind phase(average of weeks 3,6,9,12 values).
Measured: weeks 0,3,6,9,12,14,16
Mean Change in Subject-reported Daytime Alertness Averaged Over the 12 Week Double Blind Study Period
Daytime alertness was rated by study participants on a scale of 0-10, with higher scores representing better alertness. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Daytime Alertness at Various Study Time Points
Daytime alertness was rated by study participants on a scale of 0-10, with higher scores representing better alertness. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Daytime Alertness at Various Study Time Points.
Daytime alertness was rated by study participants on a scale of 0-10, with higher scores representing better alertness. Mean values reported: baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), and the average for the double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-Reported Ability to Function Averaged Over the 12 Week Double Blind Period
Ability to function was rated by study participants on a scale of 0-10, with higher scores representing better ability to function. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Ability to Function at Various Study Time Points
Ability to function was rated by study participants on a scale of 0-10, with higher scores representing better ability to function. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Ability to Function at Various Study Time Points
Ability to function was rated by study participants on a scale of 0-10, with higher scores representing better ability to function. Mean values reported: baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16) \& average for double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Ability to Concentrate Averaged Over the 12 Week Double Blind Study Period.
Ability to concentrate was rated by study participants on a scale of 0-10, with higher scores representing better concentration. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseliine (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Ability to Concentrate at Various Study Time Points.
Ability to concentrate was rated by study participants on a scale of 0-10, with higher scores representing better concentration. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Ability to Concentrate at Various Study Time Points
Ability to concentrate was rated by study participants on a scale of 0-10, with higher scores representing better concentration. Mean values reported: baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16) \& average for the double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Physical Well-Being Averaged Over the 12 Week Double Blind Study Period
Physical well-being was rated by study participants on a scale of 0-10, with higher scores representing better well-being. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Physical Well-being at Various Study Time Points.
Physical well-being was rated by study participants on a scale of 0-10, with higher scores representing better well-being. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Physical Well-Being at Various Study Time Points
Physical well-being was rated by study participants on a scale of 0-10, with higher scores representing better well-being. Mean values reported: baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), \& average for double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-Reported Counts of Number of Naps Per Week Averaged Over the 12 Week Double Blind Study Period
Change from baseline in the number of naps per week for subjects who napped during the baseline period. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose)- week 12
Mean Change From Baseline In Subject-Reported Counts of Number of Naps Per Week at Various Study Time Points
Change from baseline in the number of naps per week for subjects who napped during the baseline period. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-Reported Number of Naps Each Week at Various Study Time Points.
The mean number of naps per week for subjects who napped during the baseline period. Mean values are reported at baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), and the average for the double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change in Subject-Reported Total Nap Time Per Week Averaged Over the 12 Week Double Blind Study Period
Change from baseline in the total time (minutes) spent napping per week for subjects who napped during the baseline period. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-Reported Total Nap Time Per Week at Various Study Time Points.
Change from baseline in the total time (minutes) spent napping per week for subjects who napped during the baseline period. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-Reported Total Nap Time at Various Study Time Points
The total time (minutes) spent napping per week for subjects who napped during the baseline period. Mean values are reported at baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), and the average for the double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-Reported Total Nap Time Per Week as a Percent of Total Asleep Time Averaged Over the 12 Week Double Blind Study Period
Change from baseline in the total time spent napping per week stated as a percentage of the total time asleep for subjects who napped during the baseline period. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-Reported Total Nap Time Stated as a Percentage of the Total Asleep Time at Various Study Time Points
Change from baseline in the total time spent napping per week stated as a percentage of the total time asleep for subjects who napped during the baseline period. The change is calculated as value during double-blind phase(weeks 3,6,9,12), or the single-blind follow-up(week 14), or the non-drug treatment follow-up(week 16) minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-Reported Total Nap Time Per Week Stated as a Percentage of the Total Asleep Time at Various Study Time Points
Total time spent napping per week stated as a percentage of total time asleep for subjects who napped during baseline period. Mean values reported: baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week14), non-drug treatment follow-up(week 16), \& average for double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Total Sleep Time Measured by Actigraphy Averaged Over the 12 Week Double Blind Study Period
Participants who wore an actigraph wrist monitor, which monitors rest and activity cycles are included; the resultant data had total sleep time calculated by a Central Reader. The change is calculated as the average over the double blind period (average of post-dose values from weeks 1,4,7,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Total Sleep Time Measured by Actigraphy at Various Study Time Points
Change from baseline in total sleep time for the subset population who wore an actigraph wrist monitor. The actigraph monitors rest and activity cycles; the resultant data had sleep parameters calculated by a Central Reader. The change is calculated as time point value minus the baseline value.
Measured: Baseline (week 0), Weeks 1,4,7,12,13,15
Mean Total Sleep Time Measured by Actigraphy at Various Study Time Points
Total sleep time for subset who wore actigraph wrist monitor which monitors rest and activity cycles, sleep parameters calculated by Central Reader. Mean values reported:baseline(week0), double-blind(weeks1,4,7,12), single-blind follow-up(week13), non-drug follow-up(week15) \& average for double-blind(average of weeks1,4,7,12 values).
Measured: Weeks 0,1,4,7,12,13,15
Mean Change From Baseline in Sleep Latency Measured Using Actigraphy Averaged Over the 12 Week Double Blind Study Period
Sleep latency is the time it takes to fall asleep. Participants who wore an actigraph wrist monitor to record rest and activity cycles are included; a Central Reader calculated sleep parameters. The change is calculated as the average over the double blind period (average of post-dose values from weeks 1,4,7,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Sleep Latency Measured Using Actigraphy at Various Study Time Points
Sleep latency is a measurement of the time it takes to fall asleep. Participants who wore an actigraph wrist monitor to record rest and activity cycles are included; a Central Reader calculated sleep parameters. The change is calculated as time point value minus the baseline value.
Measured: Baseline (week 0), Weeks 1,4,7,12,13,15
Mean Sleep Latency Values Measured Using Actigraphy at Various Study Time Points.
Sleep latency:measurement of time to fall asleep. Values are for subset who wore an actigraph wrist monitor which monitors rest and activity cycles; sleep parameters calculated by Central Reader.
Measured: Weeks 0,1,4,7,12,13,15
Mean Change From Baseline in Wake Time After Sleep Onset (WASO) Measured by Actigraphy Averaged Over the 12 Week Double Blind Study Period
Wake time after sleep onset is the time spent awake from sleep onset to final awakening. Change is calculated as average over double blind period (average of post-dose values from weeks 1,4,7,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Wake Time After Sleep Onset Measured Using Actigraphy at Various Study Time Points
Wake time after sleep onset is the time spent awake from sleep onset to final awakening. Participants who wore an actigraph wrist monitor to record rest and activity cycles are included; a Central Reader calculated sleep parameters. The change is calculated as time point value minus the baseline value.
Measured: Baseline (week 0), Weeks 1,4,7,12,13,15
Mean Values for Wake Time After Sleep Onset Measured Using Actigraphy at Various Study Time Points
Wake time after sleep onset is time spent awake from sleep onset to final awakening. Mean values reported: baseline(week 0), double-blind phase(weeks 1,4,7,12), single-blind follow-up(week 13), non-drug treatment follow-up(week 15) \& average for double-blind phase(average of weeks 1,4,7,12 values).
Measured: weeks 0,1,4,7,12,13,15
Mean Change From Baseline in Number of Awakenings Using Actigraphy Averaged Over the 12 Week Double Blind Study Period
Number of awakenings refers to the number of times a subject awakens between first sleep onset to final awakening. Change is calculated as average over double blind period (average of post-dose values from weeks 1,4,7,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in the Number of Awakenings Measured Using Actigraphy at Various Study Time Points.
Number of awakenings refers to the number of times a subject awakens between first sleep onset to final awakening. Participants who wore an actigraph wrist monitor to record rest and activity cycles are included; a Central Reader calculated sleep parameters. The change is calculated as time point value minus the baseline value.
Measured: Baseline (week 0), Weeks 1,4,7,12,13,15
Mean Number of Awakenings Measured Using Actigraphy at Various Study Time Points
Number of awakenings refers to the number of times a subject awakens between first sleep onset to final awakening. Mean values are reported at baseline(week 0), double-blind phase(weeks 1,4,7,12), single-blind follow-up(week 13), non-drug treatment follow-up(week 15), and the average for the double-blind phase(average of weeks 1,4,7,12 values).
Measured: Weeks 0,1,4,7,12,13,15
Mean Change From Baseline in Number of Naps Per Week Measured Using Actigraphy Averaged Over the 12 Week Double Blind Study Period
Change from baseline in the number of naps per week for subjects who napped during the baseline period. Change is calculated as the average over the double blind period (average of post-dose values from weeks 1,4,7,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in the Number of Naps Per Week Measured Using Actigraphy at Various Study Time Points
Change from baseline in the number of naps per week for subjects who napped during the baseline period. Participants who wore an actigraph wrist monitor to record rest and activity cycles are included; a Central Reader calculated sleep parameters. The change is calculated as time point value minus the baseline value.
Measured: Baseline (week 0), Weeks 1,4,7,12,13,15
Mean Number of Naps Per Week Measured Using Actigraphy at Various Study Time Points
The number of naps per week for subjects who napped during the baseline period. Mean values are reported at baseline(week 0), double-blind phase(weeks 1,4,7,12), single-blind follow-up(week 13), non-drug treatment follow-up(week 15), and the average for the double-blind phase(average of weeks 1,4,7,12 values).
Measured: Week 0,1,4,7,12,13,15
Mean Change From Baseline Total Nap Time Per Week Measured by Actigraphy Averaged Over the 12 Week Double Blind Study Period
Change from baseline in the total nap time per week for subjects who napped during the baseline period. Change is calculated as the average over the double blind period (average of post-dose values from weeks 1,4,7,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Total Nap Time Per Week Measured by Actigraphy at Various Study Time Points
Change from baseline in the total nap time per week for subjects who napped during the baseline period. Participants who wore an actigraph wrist monitor to record rest and activity cycles are included; a Central Reader calculated sleep parameters. The change is calculated as time point value minus the baseline value.
Measured: Baseline (week 0), Weeks 1,4,7,12,13,15
Mean Total Nap Time Per Week Measured by Actigraphy at Various Study Time Points.
The total nap time per week for subjects who napped during the baseline period. Mean values are reported at baseline(week 0), double-blind phase(weeks 1,4,7,12), single-blind follow-up(week 13), non-drug treatment follow-up(week 15), and the average for the double-blind phase(average of weeks 1,4,7,12 values).
Measured: Week 0,1,4,7,12,13,15
Mean Change From Baseline in Total Nap Time Per Week as a Percentage of Total Asleep Time Measured by Actigraphy and Averaged Over the 12 Week Double Blind Study Period.
Change from baseline in the total time spent napping per week as a percent of the total time asleep for subjects who napped during the baseline period. Change is calculated as the average over the double blind period (average of post-dose values from weeks 1,4,7,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Total Nap Time Per Week as a Percentage of Total Asleep Time as Measured by Actigraphy at Various Study Time Points
Change from baseline in total time spent napping per week as a percent of total time asleep for subjects who napped during the baseline period. Change is calculated as time point value minus the baseline value.
Measured: Baseline (week 0), Weeks 1,4,7,12,13,15
Mean Total Nap Time Per Week as a Percentage of Total Asleep Time Measured Using Actigraphy at Various Study Time Points
The total time spent napping per week as a percent of the total time asleep for subjects who napped during the baseline period. Mean values reported: baseline(week 0), double-blind phase(weeks 1,4,7,12), single-blind follow-up(week 13), non-drug treatment follow-up(week 15) \& average for double-blind phase(average of weeks 1,4,7,12 values).
Measured: Week 0,1,4,7,12,13,15
Mean Change From Baseline in Insomnia Severity Index Total Score Averaged Over the 12 Week Double Blind Study Period
Change from baseline in the Insomnia Severity Index Total Score which ranges from 0-28. Lower scores represent better sleep. The change is calculated as the average over the double blind period (average of post-dose values from weeks 3,6,9,12) minus the baseline value.
Measured: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Insomnia Severity Index Total Score at Various Study Time Points
Change from baseline in the Insomnia Severity Index Total Score which ranges from 0-28. Lower scores represent better sleep. The change is calculated as time point value minus the baseline value.
Measured: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Insomnia Severity Index Total Scores at Various Study Time Points
The Insomnia Severity Index Total Score ranges from 0-28. Lower scores represent better sleep. Mean values are reported at baseline(week 0), double-blind phase(weeks 3,6,9,12), single-blind follow-up(week 14), non-drug treatment follow-up(week 16), and the average for the double-blind phase(average of weeks 3,6,9,12 values).
Measured: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Physical Component Summary of the Short Form-36 Scale
Physical component summary of Short Form-36 Scale measures subject's perception of their physical health, where the normal mean for general US population is 50.Scores above/below 50 represent better than/worse than the general US population. Higher scores represent better outcomes. Change is calculated as time point value minus baseline value.
Measured: Baseline (week 0), Weeks 6, 12, 16
Mean Physical Component Summary of the Short Form-36 Scale Scores.
This scale measures subject's perception of their physical health, where the normal mean for general US population is 50.Scores above/below 50 represent better/worse than general US population. Change calculated as time point value minus baseline value: baseline(week0), double-blind (weeks 6,12)and non-drug treatment follow-up(week16).
Measured: Weeks 0,6,12,16
Mean Change From Baseline in Mental Component Summary of the Short Form-36 Scale Scores
Mental component summary of Short Form-36 Scale measures subject's perception of their physical health, where the normal mean for general US population is 50. Scores above/below 50 represent better than/worse than the general US population. Higher scores represent better outcomes. Change is calculated as time point value minus baseline value.
Measured: Baseline (week 0), Weeks 6,12,16
Mean Mental Component Summary of the Short Form-36 Scale Scores
This scale measures subject's perception of their physical health, where normal mean for general US population is 50. Scores above/below 50 represent better/worse than general US population. Change calculated: time point value minus baseline value. Mean values: baseline(week0), double-blind phase(weeks 6,12)\& non-drug treatment follow-up(week 16).
Measured: Weeks 0,6,12,16
Mean Change From Baseline in the Sheehan Disability Scale Total Score.
Sheehan Disability Scale Total Score (range 0-30)measures subject's level of disability \& includes: work/school, social life, family life/home responsibilities, days lost \&days underproductive; higher scores represent higher degree of disability/impairment. Change is calculated as time point value minus baseline value.
Measured: Baseline (week 0), Weeks 6,12,14,16
Mean Sheehan Disability Total Scores
Sheehan Disability Scale Total Score (range 0-30) measures subject's level of disability; includes work/school, social life, family life/home responsibilities, days lost, days underproductive; higher scores represent higher degree of disability/impairment. Mean values reported: baseline, double-blind(weeks 6,12)\& follow-up(weeks 14,16).
Measured: Weeks 0,6,12,14,16
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Oct 2006 (estimated)
- Study startOct 2006
- Primary completionFeb 2008
- Study completionFeb 2008
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 InsomniaStudies of the same condition, open and under way.
- 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 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 388 participants (actual)
Sponsor and investigators
- Lead sponsor
- Sumitomo Pharma America, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Medical Director, CNS, Study chair, Sumitomo Pharma America, Inc.
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00386334
- Sponsor's protocol ID
- 190-904
- Status last verified
- Feb 2016
- First submitted
- 9 Oct 2006
- Last updated
- 14 Mar 2016
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
Publications
Ancoli-Israel S, Krystal AD, McCall WV, Schaefer K, Wilson A, Claus R, Rubens R, Roth T. A 12-week, randomized, double-blind, placebo-controlled study evaluating the effect of eszopiclone 2 mg on sleep/wake function in older adults with primary and comorbid insomnia. Sleep. 2010 Feb;33(2):225-34. doi: 10.1093/sleep/33.2.225.
PubMed 20175406
Study at a glance
From the registry record, last updated by the sponsor on 14 Mar 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Long-Term Safety and Efficacy Study of Eszopiclone in Elderly Subjects With Primary Chronic Insomnia
- ClinicalTrials.gov ID
- NCT00386334
- Acronym / sponsor ID
- 190-904
- Conditions
- Insomnia
- Keywords
- insomnia, chronic, primary
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 388 participants (actual)
- Lead sponsor
- Sumitomo Pharma America, Inc.Industry (pharma, biotech, devices)
- Study start
- Oct 2006
- Primary completion
- Feb 2008 (actual)
- Study completion
- Feb 2008 (actual)
- First posted
- 11 Oct 2006 (estimated)
- Results
- Posted 2 Jun 2009
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To evaluate the long-term safety and efficacy of eszopiclone administered for 12 weeks in elderly subjects with primary chronic insomnia.Administration of eszopiclone 2 mg daily at bedtime for 12 weeks in elderly subjects with a diagnosis of primary chronic insomnia will be safe and well tolerated, improve subjective sleep measures, improve measures of Quality of Life and next day insomnia symptoms, and have no significant withdrawal central nervous system adverse events or rebound insomnia.
Detailed description
A double-blind, randomized, placebo controlled, parallel group study of eszopiclone in elderly subjects with primary chronic insomnia. The study will involve up to 9 visits and subject participation will be approximately 18 weeks. This study was previously posted by Sepracor Inc. In October 2009, Sepracor Inc. was acquired by Dainippon Sumitomo Pharma., and in October 2010, Sepracor Inc's name was changed to Sunovion Pharmaceuticals Inc.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Placebo | Placebo comparator | Drug: PlaceboWeek -2 to day 0 single blind one tablet placebo in the evening. Double blind period: Day 1 to Week 12 double blind one tablet placebo in the evening. Follow up period: two weeks (Weeks 13-14) single blind one tablet placebo in evening, and two weeks (Weeks 15-16) no drug washout. |
| Eszopiclone | Experimental | Drug: Eszopiclone, Drug: PlaceboWeek -2 to day 0 single blind one tablet placebo in evening. Double Blind period: Day 1 to Week 12 double blind one tablet 2 mg of eszopiclone in evening. Follow up period consists of two weeks (Weeks 13-14) single blind one tablet placebo in evening, and two weeks (Weeks 15-16) no drug washout. |
Who may qualify
- Ages
- 65 to 85 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Older adult
Key inclusion criteria (1 listed)
- Male and female subjects with primary chronic insomnia. Subject is otherwise in good general health, based on screening physical examination and medical history.
Key exclusion criteria (1 listed)
- Subject has recent history of known clinically significant abnormal laboratory findings.
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 |
|---|---|---|
| EszopicloneAlso: Lunesta2 mg tablet once per day in the evening | Drug | Eszopiclone |
| PlaceboTablet one per day in the evening. | Drug | Eszopiclone, Placebo |
Primary outcome
Mean Change From Baseline in Subject-Reported Total Sleep Time (TST) Averaged Over the 12 Week Double Blind Study Period.
Time frame: Baseline (week 0), Day 1 (post first dose)-12 weeks
The difference between the total sleep time at baseline and the average total sleep time over the double blind period(average of post-dose values from weeks 3,6,9,12) reported by the participant. The change is calculated as the average over the double blind period minus the baseline value.
68 secondary outcomes
Mean Change From Baseline in Subject-reported Total Sleep Time at Various Study Time Points.
Time frame: Weeks 0, 3, 6, 9, 12, 14, 16
Mean Subject-reported Total Sleep Time in Minutes at Various Study Time Points.
Time frame: Weeks 0, 3, 6, 9, 12, 14, 16
Mean Change From Baseline in Subject-reported Sleep Latency (SL) Averaged Over the 12 Week Double Blind Period.
Time frame: Baseline (week 0), Day 1 (post first dose) - Week12
Mean Change From Baseline in Subject-reported Sleep Latency at Various Study Time Points
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Sleep Latency Reported at Various Study Time Points.
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Wake Time After Sleep Onset (WASO) Averaged Over the 12 Week Double-blind Study Period.
Time frame: Baseline (week 0), Day 1 (post first dose) -week 12
Mean Change From Baseline in Subject-reported Wake Time After Sleep Onset (WASO) at Various Study Time Points.
Time frame: Baseline (week 0), weeks 3,6,9,12,14,16
Mean Subject-reported Wake Time After Sleep Onset (WASO) at Various Study Time Points
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Number of Awakenings Averaged Over the 12 Week Double Blind Study Period.
Time frame: Baseline (week 0), Day 1 (post first dose) - Week12
Mean Change From Baseline in the Number of Subject-reported Awakenings at Various Study Time Points.
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Number of Awakenings (Subject-reported) at Various Study Time Points
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Quality of Sleep Averaged Over the 12 Week Double Blind Study Period
Time frame: Baseline (week 0), Day 1 (post first dose) - Week12
Mean Change From Baseline in Subject-reported Quality of Sleep at Various Study Time Points.
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Ratings of Subject-reported Quality of Sleep at Various Study Time Points
Time frame: weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-Reported Depth of Sleep for the Average Reported During the Double-blind Period.
Time frame: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Depth of Sleep at Various Study Time Points
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Depth of Sleep at Various Study Time Points
Time frame: weeks 0,3,6,9,12,14,16
Mean Change in Subject-reported Daytime Alertness Averaged Over the 12 Week Double Blind Study Period
Time frame: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Daytime Alertness at Various Study Time Points
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Daytime Alertness at Various Study Time Points.
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-Reported Ability to Function Averaged Over the 12 Week Double Blind Period
Time frame: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Ability to Function at Various Study Time Points
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Ability to Function at Various Study Time Points
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Ability to Concentrate Averaged Over the 12 Week Double Blind Study Period.
Time frame: Baseliine (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Ability to Concentrate at Various Study Time Points.
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Ability to Concentrate at Various Study Time Points
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-reported Physical Well-Being Averaged Over the 12 Week Double Blind Study Period
Time frame: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-reported Physical Well-being at Various Study Time Points.
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-reported Physical Well-Being at Various Study Time Points
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-Reported Counts of Number of Naps Per Week Averaged Over the 12 Week Double Blind Study Period
Time frame: Baseline (week 0), Day 1 (post first dose)- week 12
Mean Change From Baseline In Subject-Reported Counts of Number of Naps Per Week at Various Study Time Points
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-Reported Number of Naps Each Week at Various Study Time Points.
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change in Subject-Reported Total Nap Time Per Week Averaged Over the 12 Week Double Blind Study Period
Time frame: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-Reported Total Nap Time Per Week at Various Study Time Points.
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-Reported Total Nap Time at Various Study Time Points
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Subject-Reported Total Nap Time Per Week as a Percent of Total Asleep Time Averaged Over the 12 Week Double Blind Study Period
Time frame: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Subject-Reported Total Nap Time Stated as a Percentage of the Total Asleep Time at Various Study Time Points
Time frame: Baseline (week 0), Weeks 3,6,9,12,14,16
Mean Subject-Reported Total Nap Time Per Week Stated as a Percentage of the Total Asleep Time at Various Study Time Points
Time frame: Weeks 0,3,6,9,12,14,16
Mean Change From Baseline in Total Sleep Time Measured by Actigraphy Averaged Over the 12 Week Double Blind Study Period
Time frame: Baseline (week 0), Day 1 (post first dose) - week 12
Mean Change From Baseline in Total Sleep Time Measured by Actigraphy at Various Study Time Points
Time frame: Baseline (week 0), Weeks 1,4,7,12,13,15
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Mar 2016.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Results publication: PubMed 20175406Ancoli-Israel S, Krystal AD, McCall WV, Schaefer K, Wilson A, Claus R, Rubens R, Roth T. A 12-week, randomized, double-blind, placebo-controlled study evaluating the effect of eszopiclone 2 mg on sleep/wake function in older adults with primary and comorbid insomnia. Sleep. 2010 Feb;33(2):225-34. doi: 10.1093/sleep/33.2.225.
Related trials for Insomnia
Recruiting
Addressing Nocturia in Older Women Utilizing Behavioral Sleep Intervention and Brief Mindfulness
Nocturia, Insomnia
Not yet recruiting
A Transdiagnostic Sleep Health Intervention for Veterans With PTSD
Stress Disorders, Post-Traumatic, Sleep Initiation and Maintenance Disorders
Recruiting
Effect of Cyclic Sighing Breathing Exercise on CRBD, Pain, and Sleep Quality in Patients Undergoing TUR
Transurethral Resection of Bladder Tumor, Transurethral Resection of the Prostate (TURP)
Recruiting
Evaluation of Cognitive Behavioral Therapy for Insomnia (CBT-I) in Individuals With Mild Traumatic Brain Injury (mTBI)
Sleep Architecture, Mild Traumatic Brain Injury
RecruitingPhase 3
A Trial to See if Daridorexant Can Help Adults and Elderly People With Insomnia Sleep Better During the Night and Function Better During the Day
Insomia Disorder
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.
Medical Director, CNS study chair
Sumitomo Pharma America, Inc.
82 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Eszopiclone in people with Insomnia, run by Sumitomo Pharma America, Inc. at 82 sites in United States.
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 14 Mar 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 82 sites in United States. 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. Some participants in this study may receive a placebo. 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 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
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 2 Jun 2009). 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?
Mean Change From Baseline in Subject-Reported Total Sleep Time (TST) Averaged Over the 12 Week Double Blind Study Period. (time frame: Baseline (week 0), Day 1 (post first dose)-12 weeks). 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 NCT00386334, 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 14 Mar 2016.