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Search / Trial NCT02905357

Heart Attack Research Program- Imaging Study

Launched by NYU LANGONE HEALTH · Sep 13, 2016

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Myocardial Infarction Imaging

ClinConnect Summary

The Heart Attack Research Program (HARP) is a study focused on understanding the causes of heart attacks in patients who have experienced a myocardial infarction (MI) but do not have blocked arteries. This study will use imaging tests to see what might be happening inside the heart and will track participants for up to 10 years to monitor for any further heart-related issues. Researchers are looking for individuals aged 21 and older who have symptoms like chest pain or related discomfort, along with certain test results indicating a heart attack.

If you join this study, you will have regular check-ups every six months to assess your health. To be eligible, you should not have significant blockages in your heart's arteries and must be willing to participate fully in the study. It's important to note that some conditions, like a recent heart procedure or certain medical histories, may exclude you from participating. This study aims to improve our understanding of heart attacks and help develop better treatments for patients like you.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Acute ischemic symptoms compatible with diagnosis of MI, such as chest pain or anginal equivalent symptoms at rest or new onset exertional anginal equivalent symptoms
  • * Objective evidence of MI (either or both of the following):
  • Elevation of troponin to above the laboratory upper limit of normal
  • ST segment elevation of ≥1mm on 2 contiguous ECG leads
  • Willing to provide informed consent and comply with all aspects of the protocol
  • Age ≥ 21 years
  • Exclusion Criteria:
  • Stenosis ≥50% of any major epicardial vessel on invasive angiography, as determined by the angiographer at the time of clinically ordered cardiac catheterization
  • History of known obstructive coronary artery disease at angiography, including history of percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG)
  • Recent use of vasospastic agents, such as cocaine, triptans, or ergot alkaloids (≤1 month)
  • Alternate explanation for troponin elevation, such as hypertensive urgency, acute exacerbation of heart failure, chronic elevation due to kidney disease, pulmonary embolism, cardiac trauma
  • Coronary dissection apparent on angiography
  • Excessive coronary tortuosity which, in the angiographer's opinion, increases the risks of OCT
  • eGFR\<45 or contraindication to additional contrast needed for OCT in the opinion of the angiographer or treating physician
  • Contraindication to MRI (including but not limited to ferromagnetic implants)
  • Pregnancy
  • Thrombolytic therapy for STEMI (qualifying event)

About Nyu Langone Health

NYU Langone Health is a premier academic medical center located in New York City, renowned for its commitment to advancing healthcare through innovative research and clinical excellence. As a leading sponsor of clinical trials, NYU Langone Health integrates cutting-edge scientific inquiry with patient-centered care, striving to develop new therapies and improve health outcomes across a wide range of medical conditions. The institution is dedicated to fostering collaboration among researchers, clinicians, and patients, ensuring rigorous adherence to ethical standards and regulatory guidelines in all clinical research initiatives. By leveraging its extensive resources and expertise, NYU Langone Health aims to contribute significantly to the advancement of medical knowledge and the enhancement of patient care.

Locations

Stanford, California, United States

Los Angeles, California, United States

Pittsburgh, Pennsylvania, United States

Winnipeg, Manitoba, Canada

Vancouver, British Columbia, Canada

Columbus, Ohio, United States

Atlanta, Georgia, United States

Edmonton, Alberta, Canada

Baltimore, Maryland, United States

Vancouver, British Columbia, Canada

San Diego, California, United States

Birmingham, Alabama, United States

New York, New York, United States

Calgary, , Canada

Bethlehem, Pennsylvania, United States

Mineola, New York, United States

New York, New York, United States

Gainesville, Florida, United States

Lebanon, New Hampshire, United States

Austin, Texas, United States

Patients applied

0 patients applied

Trial Officials

Harmony R Reynolds, MD

Principal Investigator

NYU Langone Medical Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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