Hip FracturesHIP ATTACK-2NCT04743765
HIP Fracture Accelerated Surgical TreaTment And Care tracK 2 Trial
A study testing Accelerated medical clearance and surgery in people with Hip Fractures and Myocardial Injury, run by Population Health Research Institute at 77 sites in 20 countries.
Trial summary
The HIP ATTACK-2 trial is a multicentre, international, parallel group randomized controlled trial to determine whether accelerated surgery for hip fracture in patients with acute myocardial injury is superior to standard care in reducing death at 90 days after randomization. Read more about this study
- Who is it for?
- Ages 45 years and older
- Conditions the study is for
- Hip Fractures, Myocardial Injury
- What is being tested?
- Accelerated medical clearance and surgery
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,100 participants
- Where
- 77 sitesin 20 countries
- Study dates
- 22 Nov 2021to 30 Nov 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 45 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- age ≥45 years;
- diagnosis of hip fracture during working hours with a low-energy mechanism requiring surgery;
- troponin elevation ( at least one troponin measurement above the upper limit of normal occurring from the time of hip fracture to the time of randomization); and
- informed consent.
Who cannot join
- taking a therapeutic dose of an anticoagulant for which no reversing agent is available and the anesthesiologist or surgeon believe surgery within 6 hours of eligibility criteria met would not be safe;
- patients on a therapeutic vitamin K antagonist with a history of heparin induced thrombocytopenia (HIT);
- patients with peri-prosthetic fracture, open fracture or bilateral fractures;
- patients requiring an emergency surgery for another reason (e.g., subdural hematoma);
- patients with acute myocardial infarction deemed to be clinically unstable, with a mechanical complication (i.e., acute papillary muscle rupture, ventricular septal defect), ST elevation myocardial infarction, or cardiogenic shock;
- patients refusing consent; or
- patients previously enrolled in HIP ATTACK-2.
Trial locations and contacts
77 sites in 20 countries. Contact the study team or a site near you to ask about taking part.
77 sites in 20 countries
United States23 sites
- Active, not recruiting
University of Michigan
Ann Arbor, Michigan, 48109
- Active, not recruiting
Emory University at Grady Memorial Hospital
Atlanta, Georgia, 30322
- Active, not recruiting
University of Maryland
Baltimore, Maryland, 20742
- Active, not recruiting
Sinai Hospital of Baltimore
Baltimore, Maryland, 21215
- Active, not recruiting
St. Luke's University Health Network
Bethlehem, Pennsylvania, 18015
- Active, not recruiting
Tufts Medical Center
Boston, Massachusetts, 02111
- Active, not recruiting
Lahey Hospital and Medical Center
Burlington, Massachusetts, 01805
- Active, not recruiting
Chandler Regional Medical Center
Chandler, Arizona, 85224
- Active, not recruiting
Cleveland Clinic
Cleveland, Ohio, 44195
- Active, not recruiting
The University of Texas Southwestern Medical Center (UTSW)
Dallas, Texas, 75390
- Active, not recruiting
The Regents of the University of California
Davis, California, 95618
- Active, not recruiting
The University of Texas Health Science Center at Houston
Houston, Texas, 77030
- Active, not recruiting
University of California, Irvine
Irvine, California, 92697
- Active, not recruiting
University Medical Center of Southern Nevada
Las Vegas, Nevada, 89102
- Active, not recruiting
Dartmouth-Hitchcock Medical Center
Lebanon, New Hampshire, 03756
- Active, not recruiting
Bryan Medical Center
Lincoln, Nebraska, 68506
- Active, not recruiting
University of Wisconsin
Madison, Wisconsin, 53715
- Active, not recruiting
Froedtert Hospital
Milwaukee, Wisconsin, 53226
- Active, not recruiting
Yale New Haven Hospital
New Haven, Connecticut, 06520
- Active, not recruiting
Oregon Health and Science University
Portland, Oregon, 97239
- Active, not recruiting
Mayo Clinic
Rochester, Minnesota, 55905
- Active, not recruiting
University of Utah
Salt Lake City, Utah, 84112
- Active, not recruiting
Montefiore Medical Center
The Bronx, New York, 10467
Spain11 sites, 9 recruiting
- Recruiting
Hospital Universitari Sagrat Cor
Barcelona, Barcelona, 08029
Maria del Mar Marti Ejarque, 34 + 933 22 11 11, mmmarti@quironsalud.es
Laura Ruiz-Villa, MD
- Recruiting
Hospital Universitari Vall d'Hebron
Barcelona, Barcelona, 08035
Yaiza Garcia, 34 + 934 89 30 00, yaiza.garcia@vhir.org
Ernesto Guerra-Farfan, MD
- Recruiting
Hospital Clinic of Barcelona
Barcelona, Barcelona, 08036
Montsant Jornet Gibert, MD, 34 + 932 27 54 00, jornet@clinic.cat
Marina Renau Cerrillo, MD
- Active, not recruiting
Hospital de la Santa Creu I Sant Pau
Barcelona, Barcelona, 08041
- Recruiting
Parc Sanitari Sant Joan de Déu
Barcelona, 08830
Judit Lopez Luque, 34 + 936 61 52 08, juid.lopez@sjd.es
Juan Castellanos, MD
- Recruiting
Hospital Universitario Ramón y Cajal
Madrid, 28034
Yolanda Diez Remesal, 34 + 913 36 80 00, yolan10@gmail.com
Yolanda Diez Remesal, MD
- Recruiting
Hospital Costa del Sol
Marbella, Malaga, 29603
Alicia Lopez, 34 + 951 97 66 69, alicia.lopez@ibima.eu
Enrique Guerado, MD
- Active, not recruiting
Hospital Universitari Parc Tauli
Sabadell, Barcelona, 08208
- Recruiting
Hospital Sant Camil
Sant Pere de Ribes, Barcelona, 08810
Alfred Dealbert, MD, 34 + 938 96 00 25, adealbert@csg.cat
Alfred Dealbert, MD
- Recruiting
Hospital Universitario Mutua de Terrassa
Terrassa, Barcelona, 08221
Judit Lopez, 34 + 937 36 50 50, jlopezcatena@mutuaterrassa.cat
Marti Bernaus, MD
- Recruiting
Hospital Clinico Universitario de Vallad
Valladolid, Valladolid, 47007
Adela Pereda, 34 + 983 42 00 00, aperedama@gmail.com
Hector Aguado, MD
Canada7 sites, 6 recruiting
- Active, not recruiting
University of Alberta Hospital
Edmonton, Alberta, T6G 2B7
- Recruiting
St. Joseph's Healthcare Hamilton
Hamilton, Ontario, L8N 4A6
Krysten Gregus, 905-521-2100, gregus@hhsc.ca
Flavia Borges, MD
- Recruiting
Juravinski Hospital
Hamilton, Ontario, L8V 1C3
Krysten Gregus, 905-521-2100, gregus@HHSC.ca
Ameen Patel, MD
- Recruiting
CISSS de Laval
Laval, Quebec, H7M 3L9
Zoe Masset, 450-668-1010, zoe.masset.cissslav@ssss.gouv.qc.ca
Maxime Beaumont-Courteau, MD
- Recruiting
Victoria Hospital
London, Ontario, N6A 5W9
Fatma Alqahwaji, 519-685-8500, Fatma.alqahwaji@lhsc.on.ca
Reem Ansari, Reem.Ansari@lhsc.on.ca
- Recruiting
Markham Stouffville Hospital
Markham, Ontario, L3P 7P3
Michelle Dimas, 905-472-7373, mdimas@oakvalleyhealth.ca
Steve McMahon, MD
- Recruiting
Ottawa General Hospital
Ottawa, Ontario, K1H 8L6
Katie Mcliquham, 613-722-7000, kmcilquham@ohri.ca
Robert Feibel, MD
Pakistan7 sites, 6 recruiting
- Recruiting
Maroof International Hospital
Islamabad, ICT, 44000
Saboora Waris, MD, 92 + 51-111-644-911, saboora.waris@maroof.com.pk
Hassan Mumtaz, hassan.mumtaz@maroof.com.pk
- Recruiting
Shifa International Hospitals Ltd.
Islamabad, ICT, 44000
Tehreem Zahid, MD, 92 + 51-846-4646, dr.tehreemzahid@gmail.com
Sundus Dadan, MD, dada.sundus01@gmail.com
- Recruiting
Aga Khan University
Karachi, Sindh, 74800
Nida Zehra, 92 + 21 111 911 911, nida.zehra@aku.edu
Bisma Zubair, bisma.zubair@aku.edu
- Recruiting
Indus Hospital & Health Network
Karachi, Sindh
Ayaz Mansoor, MD, 92 + 021 35112709, ayaz.mansoor@tih.org.pk
Areeba Jabeen, MD, areeba.jabeen@tih.org.pk
- Active, not recruiting
Ghurki Trust Teaching Hospital
Lahore, Punjab Province, 54000
- Recruiting
Hayat Abad Medical Complex
Peshawar, KPK, 25000
Muhammad Waqar, MD, 92 + 091-9217140-47, wkhan43@gmail.com
Muhammad Arif, MD
- Recruiting
Combined Military Hospital
Rawalpindi, Punjab Province, 46000
Ahmed Mushtaq Khan, MD, 92 + 51 9273426, surgeon760@gmail.com
Muhammad Asif Rasheed, MD, asifmalik256@hotmail.com
India5 sites, 3 recruiting
- Active, not recruiting
Government TD Medical College
Alappuzha, Kerala, 688005
- Recruiting
Bangalore Baptist Hospital
Bangalore, Karnataka, 560024
Praveena Stanislas, 91 + 804-640-4700, praveebio@gmail.com
Tatarao Rao, tatarao777@gmail.com
- Recruiting
All India Institute of Medical Sciences (AIIMS)
New Delhi, National Capital Territory of Delhi, 110029
Nasim Mansoori, MD, 91+885-118-7292, nasim.aiims@gmail.com
Vijay Sharma, MD
- Recruiting
JIPMER
Puducherry, Puducherry, 605006
Avinash Anantharaj, MD, 91 + 772-805-0413, dravinash@gmail.com
Ranjith Kumar Mekala, MD
- Active, not recruiting
Government Medical College
Trivandrum, Kerala, 695011
Italy4 sites, 4 recruiting
- Recruiting
Galliera Hospital
Genova, 16128
Claudia Brusasco, MD, 39 + 010-56321, claudia.brusasco@galliera.it
Maria Laura Raimondo, MD
- Recruiting
Ospedale San Raffaele S.r.l.
Milan, 20132
Giacomo Placella, MD, 39 + 02-26431, placella.giacomo@hsr.it
Vincenzo Salini, MD
- Recruiting
Ospedale Galeazzi SpA
Milan, 20157
Dario Pellegrino, 39 + 02-8350-0010, dar.pellegrini@gmail.com
Serena Favoro, 39 + 02-8350-0010, Serena.Favaro@grupposandonato.it
- Recruiting
Hospital of Perugia
Perugia, Umbria, 06129
Marta Baroni, MD, 39 + 075-5781, marta.baroni@ospedale.perugia.it
Carmelinda Ruggiero, MD
Chile2 sites, 2 recruiting
- Recruiting
Pontifica Universidad Catolica de Chile
Santiago, RM, 83300024
Karen Azagra, 56 + 2-2633-2051, karen.azagra@uc.cl
Fernando Altermatt, MD
- Recruiting
Clinica Santa Maria
Santiago, 7520378
Javiera Vasquez, MD, 56 + 2-2913-0000, javiera.vasquezm@gmail.com
David Torres, MD
Finland2 sites, 1 recruiting
- Active, not recruiting
South Karelia Central Hospital
Lappeenranta, 53130
- Recruiting
Tampere University Hospital
Tampere, 33521
Aleksi Reito, MD, 358 + 3-311611, Aleksi.reito@pshp.fi
Aleksi Reito, MD
Mexico2 sites
- Active, not recruiting
Christus Muguerza del Parque
Chihuahua City, Chihuahua, 31000
- Active, not recruiting
Cruz Verde Guadalajara
Guadalajara, Jalisco, 44410
Netherlands2 sites, 2 recruiting
- Recruiting
Stichting OLVG
Amsterdam, 1091
Esther Scheibeler, 31 + 20-599-9111, E.Scheijbeler@olvg.nl
Okke Hoonhout, MD, O.hoonhout@olvg.nl
- Recruiting
Deventer Hospital
Deventer, Overijssel, 7416 SE
Ellie Landman, 31 + 570-535-353, e.b.m.landman@dz.nl
Ydo Kleinlugtenbelt, MD
South Africa2 sites, 1 recruiting
- Active, not recruiting
Stellenbosch University - Tygerberg Hospital
Cape Town, Western Cape, 7505
- Recruiting
Groote Schuur Hospital
Cape Town, Western Cape, 7925
Simphiwe Gumede, 27 + 21 404 9111, simphiwe.gumede@uct.ac.za
Sithombo Maqungo, MD
United Kingdom2 sites, 2 recruiting
- Recruiting
Chelsea and Westminster Hospital
London, SW10 9NH
Julie Logan, 44 + 20-3315-8000, julie.logan11@nhs.net
Laura Martins, 44 + 20-3315-8000, l.martins2@nhs.net
- Recruiting
West Middlesex University Hospital
Middlesex, TW7 6AF
Amrinder Sayan, 44+ 208-321-5181, amrinder.sayan@nhs.net
Jamie Gonzales, 44 + 208-321-5181, jamie.gonzales@nhs.net
Australia1 site, 1 recruiting
- Recruiting
The John Hunter Hospital
New Lambton Heights, New South Wales, 2305
Debra McDougall, 61 + 2-4921-3000, Debra.McDougall@health.nsw.gov.au
Zsolt Balogh, MD
Belgium1 site
- Active, not recruiting
Cliniques Universitaires Saint Luc - University Catholic of Louvain
Woluwe-Saint-Lambert, Brussels Capital, 1200
Brazil1 site, 1 recruiting
- Recruiting
University of São Paulo
São Paulo, São Paulo, 05403010
Maria (Adelaide) Gongalves, MD, 55 + 11-3091-3116, Adelaidemiranda99@gmail.com
Kodi Kojima, MD
Hong Kong1 site, 1 recruiting
- Recruiting
Queen Mary Hospital
Hong Kong
Grace Ho, 852 + 2255-3838, gracehpy@hku.hk
Christian Fang, MD
Malaysia1 site, 1 recruiting
- Recruiting
University of Malaya Medical Centre
Kuala Lumpur, 59100
Shwen Nee Chong, MD, 60 + 3-7949-4422, swhennee@gmail.com
Chew Yin Wang, MD
Nepal1 site, 1 recruiting
- Recruiting
B and B Hospital
Lalitpur, Bagmati, 44700
Satish Prasad Barnawal, MD, 977 + 1-5970999, satishprasadbarnawal@gmail.com
Bibek Banskota, MD
Poland1 site, 1 recruiting
- Recruiting
SPZOZ Myslenice
Myślenice, Malopolska, 32-400
Ilona Nowak-Kózka, 48 + 12-273-03-55, ilonnowak@gmail.com
Mateusz Sitkowski, mateusz.sitkowski@yahoo.com
Saudi Arabia1 site, 1 recruiting
- Recruiting
King Faisal Specialist Hospital
Riyadh, Riyadh Region, 11211
Fahad Alotaibi, 966 + 11 464 7272, falotaibi7@kfshrc.edu.sa
Husam Alrumaih, MD
About this study
Official title: HIP Fracture Accelerated Surgical TreaTment And Care tracK 2 (HIP ATTACK-2) Trial
The HIP ATTACK-2 trial is a multicentre, international, parallel group randomized controlled trial to determine whether accelerated surgery for hip fracture in patients with acute myocardial injury is superior to standard care in reducing death at 90 days after randomization. The trial will also assess secondary outcomes at 90 days after randomization: inability to independently walk 3 metres, time to first mobilization (first standing and first full weight bear), composite and individual assessment of major complications (e.g., mortality, non-fatal myocardial infarction, acute congestive heart failure, and stroke), delirium, length of stay, pain, and quality of life.
- Conditions
- Hip Fractures, Myocardial Injury
- Being tested
- Accelerated medical clearance and surgery
- Medical subject headings
- Hip Fractures
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Accelerated medical clearance and surgeryOther
Rapid medical clearance with targeted arrival to the operating room within 6 hours of eligibility criteria criteria met.
| Study group | Role | What they receive |
|---|---|---|
| Accelerated medical clearance and surgery | Experimental | Accelerated medical clearance and targeted arrival to the operating room within 6 hours of eligibility criteria met. Receives: Other: Accelerated medical clearance and surgery |
| Standard surgical care | No intervention | Hip fracture repair and surgical care according to treating institution guidelines. |
What is being measured
The primary outcome is the main question the study is designed to answer.
All cause mortality
Death due to all causes
Measured: Within 90 days post randomization
Secondary outcomes (10)
Ability to independently walk 3 meters
Ability to independently walk 3 meters (10 feet) or across a room without human assistance. Patients who require a cane or walker, but not human assistance, will be classified as able to walk independently. Patients who require assistance to get out of a chair, but can walk independently once they get up, will be classified as able to walk independently.
Measured: Within 90 days post randomization
Composite of major complications
Composite includes vascular and nonvascular mortality, non-fatal myocardial infarction, acute congestive heart failure, and stroke.
Measured: Within 90 days post randomization
Vascular mortality
Any death with a vascular cause and includes those deaths following a myocardial infarction, sudden cardiac arrest, stroke, cardiac revascularization procedure (i.e., percutaneous coronary intervention [PCI] or coronary artery bypass graft [CABG] surgery), heart failure, pulmonary embolus, cardiovascular hemorrhage, or deaths due to an unknown cause
Measured: Within 90 days post randomization
Nonvascular mortality
Any death due to a clearly documented non-vascular cause.
Measured: Within 90 days post randomization
Myocardial Infarction
Diagnosis of MI according to 4th universal definition of myocardial infarction
Measured: Within 90 days post randomization
Acute Congestive Heart Failure
at least one clinical sign(s) or symptom(s) (e.g elevated jugular venous pressure, respiratory rales/crackles, crepitations, hypoxia, tachypnea or presence of S3) with at least one of the following:
- radiographic findings (i.e., vascular redistribution, interstitial pulmonary edema, or frank alveolar pulmonary edema) or point of care ultrasound findings (i.e., bilateral B-lines, bilateral pleural effusion, elevated jugular venous pressure, dilated inferior vena cava with respiratory variation less than 50%) OR
- heart failure treatment implemented with diuretics with documented clinical improvement.
Measured: Within 90 days post randomization
Stroke
Either - 1. a new focal neurological deficit thought to be vascular in origin with signs or symptoms lasting more than 24 hours or leading to death; or 2. a new focal neurological deficit thought to be vascular in origin with signs or symptoms lasting less 24 hours with a positive neuroimaging consistent with a stroke
Measured: Within 90 days post randomization
Time from randomization to hospital discharge
Length of hospital stay from randomization to hospital discharge
Measured: Within 90 days post randomization
Delirium
- Patient meets the criteria for delirium on any in-person 3D-CAM or CAM administered; OR
- Positive history of delirium in the 7 days after randomization based on the review of hospital health records.
Measured: Within 7 days and 90 days post randomization
Moderate to severe pain
Moderate to severe pain is defined as any pain score ≥3 on 10 points scale.
Measured: Within 7 days and 90 days post randomization
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Feb 2021
- Study start22 Nov 2021
- Primary completion31 Aug 2027 (estimated)
- Study completion30 Nov 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hip FracturesStudies 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 N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 1,100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Population Health Research Institute
- Sponsor type
- University, hospital or other
- Collaborators
- Canadian Institutes of Health Research (CIHR), National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
- Responsible party
- Sponsor
- Investigators
- Flavia Borges, M.D, Principal investigator, Population Health Research InstituteGerard Slobogean, M.D, Principal investigator, UC IrvineRobert Feibel, M.D, Principal investigator, The Ottawa HospitalPJ Devereaux, M.D, Study chair, Population Health Research Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04743765
- Sponsor's protocol ID
- v2.0_20230608
- Acronym
- HIP ATTACK-2
- Status last verified
- Sep 2025
- First submitted
- 3 Feb 2021
- Last updated
- 26 Aug 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: The Population Health Research Institute (PHRI) is the sponsor of this trial. The PHRI believes the dissemination of clinical research results is vital and sharing of data is important. PHRI prioritizes access to data analyses to researchers who have worked on the trial for a significant duration, have played substantial roles, and have participated in raising the funds to conduct the trial. PHRI balances the length of the research study, and the intellectual and financial investments that made it possible with the need to allow wider access to the data collected. Data will be disclosed only upon request and approval of the proposed use of the data by a Review Committee.
Study at a glance
From the registry record, last updated by the sponsor on 26 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- HIP Fracture Accelerated Surgical TreaTment And Care tracK 2 (HIP ATTACK-2) Trial
- ClinicalTrials.gov ID
- NCT04743765
- Acronym / sponsor ID
- HIP ATTACK-2 / v2.0_20230608
- Conditions
- Hip Fractures, Myocardial Injury
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 1,100 participants (estimated)
- Lead sponsor
- Population Health Research InstituteUniversity, hospital or other
- Collaborators
- Canadian Institutes of Health Research (CIHR), National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
- Study start
- 22 Nov 2021 (actual)
- Primary completion
- 31 Aug 2027 (estimated)
- Study completion
- 30 Nov 2027 (estimated)
- First posted
- 8 Feb 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The HIP ATTACK-2 trial is a multicentre, international, parallel group randomized controlled trial to determine whether accelerated surgery for hip fracture in patients with acute myocardial injury is superior to standard care in reducing death at 90 days after randomization. The trial will also assess secondary outcomes at 90 days after randomization: inability to independently walk 3 metres, time to first mobilization (first standing and first full weight bear), composite and individual assessment of major complications (e.g., mortality, non-fatal myocardial infarction, acute congestive heart failure, and stroke), delirium, length of stay, pain, and quality of life.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Accelerated medical clearance and surgery | Experimental | Other: Accelerated medical clearance and surgeryAccelerated medical clearance and targeted arrival to the operating room within 6 hours of eligibility criteria met. |
| Standard surgical care | No intervention | –Hip fracture repair and surgical care according to treating institution guidelines. |
Who may qualify
- Ages
- 45 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- age ≥45 years;
- diagnosis of hip fracture during working hours with a low-energy mechanism requiring surgery;
- troponin elevation ( at least one troponin measurement above the upper limit of normal occurring from the time of hip fracture to the time of randomization); and
- informed consent.
Key exclusion criteria (7 listed)
- taking a therapeutic dose of an anticoagulant for which no reversing agent is available and the anesthesiologist or surgeon believe surgery within 6 hours of eligibility criteria met would not be safe;
- patients on a therapeutic vitamin K antagonist with a history of heparin induced thrombocytopenia (HIT);
- patients with peri-prosthetic fracture, open fracture or bilateral fractures;
- patients requiring an emergency surgery for another reason (e.g., subdural hematoma);
- patients with acute myocardial infarction deemed to be clinically unstable, with a mechanical complication (i.e., acute papillary muscle rupture, ventricular septal defect), ST elevation myocardial infarction, or cardiogenic shock;
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 |
|---|---|---|
| Accelerated medical clearance and surgeryRapid medical clearance with targeted arrival to the operating room within 6 hours of eligibility criteria criteria met. | Other | Accelerated medical clearance and surgery |
Primary outcome
All cause mortality
Time frame: Within 90 days post randomization
Death due to all causes
10 secondary outcomes
Ability to independently walk 3 meters
Time frame: Within 90 days post randomization
Composite of major complications
Time frame: Within 90 days post randomization
Vascular mortality
Time frame: Within 90 days post randomization
Nonvascular mortality
Time frame: Within 90 days post randomization
Myocardial Infarction
Time frame: Within 90 days post randomization
Acute Congestive Heart Failure
Time frame: Within 90 days post randomization
Stroke
Time frame: Within 90 days post randomization
Time from randomization to hospital discharge
Time frame: Within 90 days post randomization
Delirium
Time frame: Within 7 days and 90 days post randomization
Moderate to severe pain
Time frame: Within 7 days and 90 days post randomization
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Aug 2026.
- Individual participant dataSharing planned: No. The Population Health Research Institute (PHRI) is the sponsor of this trial. The PHRI believes the dissemination of clinical research results is vital and sharing of data is important. PHRI prioritizes access to data analyses to researchers who have worked on the trial for a significant duration, have played substantial roles, and have participated in raising the funds to conduct the trial. PHRI balances the length of the research study, and the intellectual and financial investments that made it possible with the need to allow wider access to the data collected. Data will be disclosed only upon request and approval of the proposed use of the data by a Review Committee.
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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.
Flavia Borges, M.D principal investigator
Population Health Research Institute
Gerard Slobogean, M.D principal investigator
UC Irvine
Robert Feibel, M.D principal investigator
The Ottawa Hospital
77 sites in 20 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Accelerated medical clearance and surgery in people with Hip Fractures and Myocardial Injury, run by Population Health Research Institute at 77 sites in 20 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 4 inclusion and 7 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: looking for participants now, as of the sponsor's last update on 26 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 77 sites in United States, Spain, Canada, Pakistan, India and 15 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.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Valerie Harvey (905-297-3479 ext. 40793, valerie.harvey@phri.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
All cause mortality (time frame: Within 90 days post randomization). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 26 Aug 2026.