NCT05288361Active, not recruiting
The DISCOVER INOCA Prospective Multi-center Registry
Determining the Cause of Coronary Vasomotor Disorders in Patients With Ischemia and No Obstructive Coronary Artery Disease
Source: ClinicalTrials.gov · Last updated 23 Oct 2026
Brief summary (registry, in English)
The overall objective of this multi-center registry is to identify specific phenotypes of INOCA with both an anatomic evaluation (coronary angiography and intravascular imaging) and physiologic assessment with the Abbott Coroventis Coroflow Cardiovascular System, and to determine long-term outcomes.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 500 (estimated)
- First submitted
- 9 Mar 2022
- Start date
- 14 Sept 2022
- Primary completion date
- 31 Dec 2032
- Lead sponsor
- Yale University
- Diseases
- Coronary artery disease
- NCT number
- NCT05288361
What you commit to
- Study type: Observational
- Planned participants: 500
- From 14 Sept 2022 to the primary completion date, 31 Dec 2032
- 9 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior percutaneous coronary intervention
- Prior coronary artery bypass graft surgery
- Prior ST-elevation myocardial infarction
- Current or planned participation in a study of an investigational therapy
Other illness
- History of hypertrophic cardiomyopathy
- History of infiltrative heart disease (e.g., cardiac amyloidosis)
- New York Heart Association Class IV congestive heart failure
- Severe pulmonary hypertension (Mean pulmonary artery pressure greater than or equal to 35mmHg or echocardiographic right ventricular systolic pressure greater than or equal to 60mmHg)
- Known history of unrepaired or repaired congenital heart disease
- Past or pending heart transplant, or on the waiting list for organ transplant
- Known other medical illness or known history of substance abuse that may cause non-compliance with the protocol, or is associated with a life expectancy of less than 1 year
Lab values
- Any myocardial infarction at index presentation or within 90 days prior to enrollment, defined as any electrocardiogram diagnostic for myocardial infarction OR elevation in serum troponin greater than the upper limit of the site-defined reference range
- Known left ventricular ejection fraction \< 50% or cardiogenic shock requiring pressors or mechanical circulatory assistance (e.g., intra-aortic balloon pump, left ventricular assist device, other temporary cardiac support blood pump)
- Renal insufficiency, defined as estimated glomerular filtration rate (eGFR) \<30 mL/min/1.73 m2 (by the Modification of Diet in Renal Disease equation) or dialysis at the time of screening
Other
- Pregnant or nursing
- Planned percutaneous coronary intervention (PCI)
- Severe mitral regurgitation
- Severe aortic stenosis
- Angiographic stenosis in any major epicardial vessel ≥ 70% by visual estimate
- Angiographic stenosis in any major epicardial vessel greater than or equal to 50% and \< 70% by visual estimate with FFR less than or equal to 0.80 or RFR less than or equal to 0.89
Who the study is looking for
- Suspected ischemic heart disease and is referred to undergo clinically indicated invasive coronary angiography
- No obstructive coronary artery disease (CAD) as defined by operator visual assessment with (1) angiographically normal coronary arteries OR (2) non-obstructive CAD with angiographic stenosis \< 50%, or greater than or equal to 50 but \< 70% with FFR greater than or equal to 0.81 or RFR greater than or equal to 0.90
- Willing to comply with specified follow-up evaluations. The participant or legally authorized representative has been informed of the nature of the study, agrees to its provisions, and has been provided written informed consent approved by the appropriate Institutional Review Board (IRB) or Ethics Committee (EC)
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (9)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| New York-Presbyterian/Brooklyn Methodist Hospital Coordinator of this site? Confirm its status | Brooklyn | United States | Unknown status |
| The Christ Hospital Coordinator of this site? Confirm its status | Cincinnati | United States | Unknown status |
| Northeast Georgia Medical Center Coordinator of this site? Confirm its status | Gainesville | United States | Unknown status |
| UCLA Health Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Yale New Haven Hospital Coordinator of this site? Confirm its status | New Haven | United States | Unknown status |
| Columbia University Irving Medical Center Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| NYU Langone Health Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Thomas Jefferson University Hospital Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| Stanford Hospital Coordinator of this site? Confirm its status | Stanford | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.