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Search / Trial NCT04743765

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.

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

0 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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