Pre-emptive, OCT guided angioplasty of vulnerable, intermediate coronary lesions: a randomized trial, the ‘PECTUS’ Trial
Recruiting
- Conditions
- Coronary artery diseasevulnerable plaque
- Registration Number
- NL-OMON26010
- Lead Sponsor
- VU University Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 500
Inclusion Criteria
· Informed consent must be obtained
Exclusion Criteria
· Refusal or inability to provide informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A composite of major adverse cardiovascular events (all cause mortality, non-fatal myocardial infarction (STEMI or NSTEMI), or unplanned revascularization) at one year follow-up
- Secondary Outcome Measures
Name Time Method The same composite at 2 and 5 years