I25
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - patients undergoing coronary stent implantation with indication for oral anticoagulation for at least 6 months - pretreatment with ASA and clopidogrel - planned treatment with clopidogrel and vitamin K-antagonist following percutaneous coronary intervention - age >=18 years - written informed consent
Exclusion criteria
Exclusion criteria: - high-risk acute coronary syndrome (because usually treated with triple therapy) - fibrinolysis or GP IIb/IIIa antagonist with 5 days before enrollment - contraindication for clopidogrel or vitamin K-antagonist -thrombopenia - known severe coagulopathy - severe disease leading to a life expectancy of less than 1 year
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| death or non-fatal myocardial infarction within 6 months following coronary stent implantation | — |
Secondary
| Measure | Time frame |
|---|---|
| prevalence of high on-treatment platelet reactivity further ischemic endpoints such as urgent revascularization | — |
Countries
Germany
Contacts
Universitäts-Herzzentrum Freiburg Bad KrozingenKlinik für Kardiologie und Angiologie II