Percutaneous Coronary Intervention Registry FRIBOURG
Overview
The registry aims to follow clinically all consecutive patients treated by percutaneous coronary interventions at hospital & university Fribourg.
Study Type
- Study Type: Observational [Patient Registry]
- Study Design
- Time Perspective: Prospective
- Study Primary Completion Date: September 1, 2017
Interventions
- Device: Percutaneous coronary intervention, stents
Clinical Trial Outcome Measures
Primary Measures
- Patient-oriented composite endpoints (POCE)
- Time Frame: 2 years
- Academic Research Consortium definition
- Major Bleeding
- Time Frame: 2 years
- Bleeding Academic Research Consortium definition
- Patient-oriented composite endpoints (POCE)
- Time Frame: 5 years
- Academic Research Consortium definition
- Major Bleeding
- Time Frame: 5 years
- Bleeding Academic Research Consortium definition
- Patient-oriented composite endpoints (POCE)
- Time Frame: 10 years
- Academic Research Consortium definition
- Major Bleeding
- Time Frame: 10 years
- Bleeding Academic Research Consortium definition
Secondary Measures
- all-cause death
- Time Frame: 2 years
- Academic Research Consortium definition
- any revascularization
- Time Frame: 2 years
- Academic Research Consortium definition
- any myocardial infarction
- Time Frame: 2 years
- Academic Research Consortium definition
Participating in This Clinical Trial
Inclusion Criteria
- All consecutive patients treated by percutaneous coronary intervention at our institution – Able to give informed consent and willing to participate Exclusion Criteria:
- Unwillingness to participate – Enable to provide inform consent
Gender Eligibility: All
Minimum Age: 17 Years
Maximum Age: 120 Years
Are Healthy Volunteers Accepted: No
Investigator Details
- Lead Sponsor
- University of Freiburg
- Provider of Information About this Clinical Study
- Principal Investigator: Stéphane Cook, Prof, Chairman, cardiology – University of Freiburg
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