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NCT06089031 | RECRUITING | Coronary Microvascular Dysfunction

Belgian Registry on Coronary Function Testing
Sponsor:

University Hospital, Antwerp

Brief Summary:

The goal of this prospective, multicenter registy is to describe the 'real-world' use of coronary function tests, which may consist of bolus thermodilution measurements of coronary microvascular function and/or invasive vasoreactivity tests with acetylcholine, in the current Belgian routine practice. The main questions it aims to answer are: * how frequent are coronary function tests performed * what is the indication for coronary function tests * what is the frequency of coronary microvascular dysfunction * what is the frequency of coronary artery vasospasm From each participant, data will be collected from their medical files concerning cardiovascular risk factors, relevant past medical history, non-invasive tests, procedural data, and follow-up data from routine in-patient visits. Their are no specific study visits. Optionally, patients will be asked to fill in questionnaires about anginal symptoms and quality of life.

Condition or disease

Coronary Microvascular Dysfunction

Coronary Artery Vasospasm

Intervention/treatment

Coronary Function Test

Study Type : OBSERVATIONAL
Estimated Enrollment : 650 participants
Official Title : A Prospective Multicenter Registry on Coronary Function Tests, Organized by the Belgian Working Group on Coronary Microcirculation/Belgian Microcirculation Registry.
Actual Study Start Date : 2021-10-18
Estimated Primary Completion Date : 2025-12-31
Estimated Study Completion Date : 2026-12-31

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Patient scheduled for coronary function test, comprising of intracoronary bolus thermodilution measurements of microvascular function, and/or intracoronary vasoreactivity tests with acetylcholine.
  • * Subject understands the study requirements and provides written informed consent.
Exclusion Criteria
  • * Subject is participating in another investigational clinical trial that may cause non-compliance with the protocol or confound data interpretation.
  • * Subject intends to participate in another investigational clinical trial that may cause non-compliance with the protocol or confound data interpretation.
  • * Documented or suspected pregnancy.
  • * Inability to provide written informed consent.
Belgian Registry on Coronary Function Testing

Location Details

NCT06089031

Please Choose a site

How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations

RECRUITING

Belgium, Antwerp

That's Monica

Door, Antwerp, Belgium, 2100

RECRUITING

Belgium, Antwerp

AZ Sint-Maarten

Mechelen, Antwerp, Belgium, 2800

RECRUITING

Belgium, Limburg

Jessa Hasselt

Hasselt, Limburg, Belgium, 3500

RECRUITING

Belgium,

OLV Aalst

Aalst, Belgium, 9300

RECRUITING

Belgium,

Hospital aan de Stroom (ZAS)

Antwerp, Belgium, 2020

RECRUITING

Belgium,

University Hospital Antwerp

Antwerp, Belgium, 2650

RECRUITING

Belgium,

AZ St. John Bruges

Brugge, Belgium, 8000

RECRUITING

Belgium,

AZ

Yolder, Belgium, 8900

RECRUITING

Belgium,

AZ Groeninge

Kortrijk, Belgium, 8500

RECRUITING

Belgium,

UZ Leuven

Leuven, Belgium, 3000

RECRUITING

Belgium,

Chc Montlégia Liège

Liège, Belgium, 4000

RECRUITING

Belgium,

CHR Citadel Liège

Liège, Belgium,

RECRUITING

Belgium,

The delta

Roeselare, Belgium, 8800