NCT06089031Recruiting
Belgian Registry on Coronary Function Testing
A Prospective Multicenter Registry on Coronary Function Tests, Organized by the Belgian Working Group on Coronary Microcirculation/Belgian Microcirculation Registry.
Source: ClinicalTrials.gov · Last updated 18 Oct 2023 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 650 (estimated)
- First submitted
- 12 Oct 2023
- Start date
- Oct 2021
- Primary completion date
- Dec 2025
- Lead sponsor
- University Hospital, Antwerp
- Diseases
- Coronary artery disease
- NCT number
- NCT06089031
What you commit to
- Study type: Observational
- Planned participants: 650
- From Oct 2021 to the primary completion date, Dec 2025
- 13 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.
Other
- 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.
Who the study is looking for
- 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.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (13)
Sites in registry order. Pick your city on the disease page to sort them by distance.
This page is information, not medical advice. Discuss any trial with your doctor.