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Active, not recruiting No phase listed Observational

Heart Attack Research Program- Imaging Study

ClinicalTrials.gov ID: NCT02905357

Public ClinicalTrials.gov record NCT02905357. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 7:41 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The HARP study is a multi-center, diagnostic observational study employing standardized imaging protocols in patients with MINOCA (MI with Non Obstructive Coronary Arteries) to determine the underlying diagnosis in each participant. Participants will be followed for recurrent clinical events, every 6 months, for a maximum of 10 years.

Study identification

NCT ID
NCT02905357
Recruitment status
Active, not recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
NYU Langone Health
Other
Enrollment
450 participants

Conditions and interventions

Interventions

Device · Other

Eligibility (public fields only)

Age range
21 Years to 99 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 11, 2016
Primary completion
Jun 29, 2027
Completion
Jun 29, 2027
Last update posted
Mar 18, 2026

2016 – 2027

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
University of Alabama-Birmingham Birmingham Alabama 35294
Cedars-Sinai Medical Center Los Angeles California 90048
UC San Diego Medical Center San Diego California 92103
Stanford University Stanford California 94305
University of Florida Medical Center Gainesville Florida 32603
Emory University Atlanta Georgia 30322
Johns Hopkins Medical Center Baltimore Maryland 21287
Dartmouth-Hitchcock Lebanon New Hampshire 03766
NYU Winthrop Mineola New York 11501
NYU Langone Medical Center New York New York 10016
Columbia University Medical Center/NYPH New York New York 10032
Ohio State University Medical Center Columbus Ohio 43210
St. Luke's University Health Network Bethlehem Pennsylvania 18015
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213
Seton Heart (Ascension) Univeristy of Austin, Texas Austin Texas 78705

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02905357, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 18, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02905357 live on ClinicalTrials.gov.

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