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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
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

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
New York-Presbyterian/Brooklyn Methodist Hospital
Coordinator of this site? Confirm its status
BrooklynUnited StatesUnknown status
The Christ Hospital
Coordinator of this site? Confirm its status
CincinnatiUnited StatesUnknown status
Northeast Georgia Medical Center
Coordinator of this site? Confirm its status
GainesvilleUnited StatesUnknown status
UCLA Health
Coordinator of this site? Confirm its status
Los AngelesUnited StatesUnknown status
Yale New Haven Hospital
Coordinator of this site? Confirm its status
New HavenUnited StatesUnknown status
Columbia University Irving Medical Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
NYU Langone Health
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Thomas Jefferson University Hospital
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
Stanford Hospital
Coordinator of this site? Confirm its status
StanfordUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.