Veiligheid en effectiviteit van PCI optimalisatie door het gebruik van hoge resolutie IVUS vergeleken met de standaard behandeling bij patiënten met een lage FFR na de procedure
Recruiting
- Conditions
- FFR, post PCI FFR, IVUS, PCI, atherosclerosis, atherosclerose, dotter, post procedurele FFR
- Registration Number
- NL-OMON25972
- Lead Sponsor
- Erasmus Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 640
Inclusion Criteria
1.Age ≥18
2.Stable- or unstable angina or Non-ST segment elevation myocardial infarction
Exclusion Criteria
1.Patients with ST-elevation myocardial infarction (STEMI) or evidence of myocardial infarction within 72 hours before the index procedure
2.Target vessel distal reference diameter <2.25mm
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Target vessel failure, defined as composite of cardiac death, target vessel Q-wave or non-Q wave myocardial infarction, coronary artery bypass graft and clinically driven target vessel revascularization.
- Secondary Outcome Measures
Name Time Method