Heart Attack Research Program- Imaging Study

Status: Recruiting
Location: See all (19) locations...
Intervention Type: Device, Other
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 21
Maximum Age: 99
Healthy Volunteers: f
View:

• 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

Locations
United States
Alabama
University of Alabama-Birmingham
COMPLETED
Birmingham
California
Cedars-Sinai Medical Center
ACTIVE_NOT_RECRUITING
Los Angeles
UC San Diego Medical Center
ACTIVE_NOT_RECRUITING
San Diego
Stanford University
ACTIVE_NOT_RECRUITING
Stanford
Florida
University of Florida Medical Center
ACTIVE_NOT_RECRUITING
Gainesville
Georgia
Emory University
ACTIVE_NOT_RECRUITING
Atlanta
Maryland
Johns Hopkins Medical Center
ACTIVE_NOT_RECRUITING
Baltimore
New Hampshire
Dartmouth-Hitchcock
ACTIVE_NOT_RECRUITING
Lebanon
New York
NYU Winthrop
RECRUITING
Mineola
Columbia University Medical Center/NYPH
COMPLETED
New York
NYU Langone Medical Center
RECRUITING
New York
Ohio
Ohio State University Medical Center
ACTIVE_NOT_RECRUITING
Columbus
Pennsylvania
St. Luke's University Health Network
ACTIVE_NOT_RECRUITING
Bethlehem
University of Pittsburgh Medical Center
ACTIVE_NOT_RECRUITING
Pittsburgh
Texas
Seton Heart (Ascension) Univeristy of Austin, Texas
ACTIVE_NOT_RECRUITING
Austin
Other Locations
Canada
University of Calgary
ACTIVE_NOT_RECRUITING
Calgary
University of Alberta
ACTIVE_NOT_RECRUITING
Edmonton
Vancouver General Hospital
ACTIVE_NOT_RECRUITING
Vancouver
St. Boniface General Hospital
ACTIVE_NOT_RECRUITING
Winnipeg
Contact Information
Primary
Harmony R Reynolds, MD
harmony.reynolds@nyumc.org
646-501-0302
Time Frame
Start Date: 2020-07-01
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 450
Treatments
MINOCA
OCT and CMR imaging
MI-CAD
Screen failures with MI found to have obstructive CAD. Limited data collection for comparison to MINOCA cohort.
Related Therapeutic Areas
Sponsors
Leads: NYU Langone Health

This content was sourced from clinicaltrials.gov