Coronary Artery Disease, Percutaneous Coronary Intervention
Conditions
Keywords
PCI
Brief summary
The registry aims to follow clinically all consecutive patients treated by percutaneous coronary interventions at hospital & university Fribourg.
Interventions
DEVICEPercutaneous coronary intervention, stents
Sponsors
University of Freiburg
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
17 Years to 120 Years
Healthy volunteers
No
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Patient-oriented composite endpoints (POCE) | 2 years | Academic Research Consortium definition |
| Major Bleeding | 2 years | Bleeding Academic Research Consortium definition |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| all-cause death | 2 years | Academic Research Consortium definition |
| any revascularization | 2 years | Academic Research Consortium definition |
| any myocardial infarction | 2 years | Academic Research Consortium definition |
Countries
Switzerland
Outcome results
None listed