Replacement of invasive diagnostic coronary procedures by innovative noninvasive Imaging Technologies
Recruiting
- Conditions
- Coronary Artery Disease Cardiac ischemiaMagnetic Resonance Imaging Cardiac computed tomographyCTAMRI
- Registration Number
- NL-OMON22758
- Lead Sponsor
- niversity Medical Center Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 440
Inclusion Criteria
All patients >18 years of age referred for ICA as part of standard clinical care for evaluation of suspected CAD
Exclusion Criteria
Major exclusion criteria are:
-Unable to provide written informed consent
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint is the performance of noninvasive imaging (combined CTA and MR perfusion) to diagnose flow-limiting CAD compared to the reference standard of ICA.
- Secondary Outcome Measures
Name Time Method Secondary endpoints include the performance of individual components of the noninvasive imaging approach, the ability to guide revascularization strategy and the prediction of improvement of perfusion after revascularization.