HIP Fracture Accelerated Surgical TreaTment And Care tracK 2 Trial
Launched by POPULATION HEALTH RESEARCH INSTITUTE · Feb 3, 2021
Trial Information
Current as of June 27, 2025
Recruiting
Keywords
ClinConnect Summary
The HIP ATTACK-2 trial is a study designed to see if having surgery sooner for hip fractures in patients who also have heart problems (specifically, an increase in heart injury markers) can help them live longer and healthier after 90 days. The trial will compare this faster surgery approach to the usual care patients receive and will look at several important factors, such as whether patients can walk independently, how quickly they can start moving after surgery, and their overall health and quality of life during this time.
To participate in this trial, you need to be at least 45 years old and have a hip fracture that needs surgery, along with elevated heart injury markers. However, certain conditions, like being on certain blood thinners or having more severe heart issues, may prevent you from joining. If you do take part, you will be closely monitored for 90 days to track your recovery and any complications, giving you a chance to contribute to important research that could improve care for future patients with similar conditions.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. age ≥45 years;
- • 2. diagnosis of hip fracture during working hours with a low-energy mechanism requiring surgery;
- • 3. 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
- • 4. informed consent.
- Exclusion Criteria:
- • 1. 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;
- • 2. patients on a therapeutic vitamin K antagonist with a history of heparin induced thrombocytopenia (HIT);
- • 3. patients with peri-prosthetic fracture, open fracture or bilateral fractures;
- • 4. patients requiring an emergency surgery for another reason (e.g., subdural hematoma);
- • 5. 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;
- • 6. patients refusing consent; or
- • 7. patients previously enrolled in HIP ATTACK-2.
About Population Health Research Institute
The Population Health Research Institute (PHRI) is a leading clinical research organization dedicated to advancing the understanding of population health through innovative research methodologies. With a focus on large-scale, multi-center clinical trials and epidemiological studies, PHRI aims to address pressing health challenges by investigating the interplay between lifestyle, genetic, and environmental factors. By fostering collaboration among researchers, healthcare providers, and communities, PHRI strives to generate evidence-based insights that inform public health policies and improve health outcomes on a global scale. Their commitment to excellence in research is underscored by a robust infrastructure and a multidisciplinary team of experts dedicated to translating research findings into actionable solutions for diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Rochester, Minnesota, United States
Ann Arbor, Michigan, United States
Bronx, New York, United States
Cleveland, Ohio, United States
Edmonton, Alberta, Canada
Baltimore, Maryland, United States
Tampere, , Finland
Lebanon, New Hampshire, United States
Hong Kong, , Hong Kong
Ottawa, Ontario, Canada
Boston, Massachusetts, United States
Portland, Oregon, United States
Burlington, Massachusetts, United States
Hamilton, Ontario, Canada
New Haven, Connecticut, United States
Terrassa, Barcelona, Spain
Madison, Wisconsin, United States
Cape Town, Western Cape, South Africa
Karachi, Sindh, Pakistan
Barcelona, , Spain
Barcelona, , Spain
Tampere, , Finland
Barcelona, , Spain
Lappeenranta, , Finland
Genova, , Italy
Chihuahua, , Mexico
Baltimore, Maryland, United States
Rawalpindi, Punjab, Pakistan
Milan, , Italy
Marbella, Malaga, Spain
London, Ontario, Canada
Bethlehem, Pennsylvania, United States
Deventer, Overijssel, Netherlands
Hamilton, Ontario, Canada
Kuala Lumpur, , Malaysia
Sabadell, Barcelona, Spain
Markham, Ontario, Canada
Milan, , Italy
Santiago, , Chile
Lincoln, Nebraska, United States
Barcelona, , Spain
Islamabad, , Pakistan
Pondicherry, , India
Trivandrum, Kerala, India
Lahore, , Pakistan
Rawalpindi, , Pakistan
Woluwe Saint Lambert, Brussels, Belgium
Sant Pere De Ribes, Barcelona, Spain
Valladolid, , Spain
Lahore, Punjab, Pakistan
New Lambton Heights, New South Wales, Australia
Guadalajara, Jalisco, Mexico
Lalitpur, Bagmati, Nepal
Riyadh, , Saudi Arabia
Myslenice, , Poland
New Delhi, Delhi, India
Islamabad, Ict, Pakistan
Peshawar, Kpk, Pakistan
Cape Town, , South Africa
Milan, , Italy
Milan, , Italy
Islamabad, Ict, Pakistan
Myslenice, Malopolska, Poland
Cape Town, Western Cape, South Africa
São Paulo, Sp, Brazil
Karachi, Sind, Pakistan
Santiago, Rm, Chile
Bangalore, Karnataka, India
Alappuzha, Kerala, India
Davis, California, United States
Amsterdam, , Netherlands
Barcelona, , Spain
Laval, Quebec, Canada
Perugia, Umbria, Italy
Patients applied
Trial Officials
Flavia Borges, M.D
Principal Investigator
Population Health Research Institute
Gerard Slobogean, M.D
Principal Investigator
University of Maryland, Baltimore
Robert Feibel, M.D
Principal Investigator
The Ottawa Hospital
PJ Devereaux, M.D
Study Chair
Population Health Research Institute
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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