Actively Recruiting
A Prospective Multicenter Registry on Coronary Function Tests Organized by the Belgian Working Group on Coronary Microcirculation
Led by University Hospital, Antwerp · Updated on 2023-10-18
650
Participants Needed
13
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are conducting a prospective, multicenter registry to observe the real-world use of coronary function tests in routine Belgian medical practice. These tests may include bolus thermodilution measurements of coronary microvascular function and invasive vasoreactivity tests using acetylcholine. The study aims to understand how often these tests are performed, the reasons for testing, and the frequencies of coronary microvascular dysfunction and coronary artery vasospasm. Participants scheduled for coronary function tests will have data collected from their medical records regarding cardiovascular risk factors, past medical history, non-invasive test results, procedural details, and follow-up visits. There are no study-specific visits planned. Optionally, participants may complete questionnaires about their anginal symptoms and quality of life. No interventions are administered as part of this observational study. Participants' involvement includes routine data collection from medical files over a follow-up period of up to five years. Researchers will measure the frequency of coronary microvascular dysfunction and coronary artery vasospasm, as well as describe predictors for these conditions and major adverse cardiovascular events over one and three years among different patient groups. The study is organized by the University Hospital, Antwerp, and aims to provide valuable insights into coronary function testing practices and outcomes.
CONDITIONS
Brief Title
Belgian Registry on Coronary Function Testing
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient scheduled for coronary function test, including bolus thermodilution measurements and/or acetylcholine vasoreactivity tests
- Subject understands the study requirements and provides written informed consent
You will not qualify if you...
- Subject is participating in another investigational clinical trial that may affect compliance or data interpretation
- Subject plans to participate in another investigational clinical trial that may affect compliance or data interpretation
- Documented or suspected pregnancy
- Inability to provide written informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo coronary function tests which may include bolus thermodilution measurements and/or acetylcholine vasoreactivity tests to assess coronary microvascular function.
1 visit (in-person)
Duration - Up to 5 years
Participants are observed for up to 5 years to monitor the frequency and predictors of coronary microvascular dysfunction and coronary artery vasospasm.
Annual visits for up to 5 years
Trial Site Locations
Total: 13 locations
1
AZ Monica
Deurne, Antwerp, Belgium, 2100
Actively Recruiting
2
AZ Sint-Maarten
Mechelen, Antwerp, Belgium, 2800
Actively Recruiting
3
Jessa Hasselt
Hasselt, Limburg, Belgium, 3500
Actively Recruiting
4
OLV Aalst
Aalst, Belgium, 9300
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5
Ziekenhuis aan de Stroom (ZAS)
Antwerp, Belgium, 2020
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6
University Hospital Antwerp
Antwerp, Belgium, 2650
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7
AZ Sint-Jan Brugge
Bruges, Belgium, 8000
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8
AZ Jan Yperman
Ieper, Belgium, 8900
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9
AZ Groeninge
Kortrijk, Belgium, 8500
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10
UZ Leuven
Leuven, Belgium, 3000
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11
CHC Montlégia Liège
Liège, Belgium, 4000
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12
CHR Citadelle Liège
Liège, Belgium
Actively Recruiting
13
AZ Delta
Roeselare, Belgium, 8800
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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