Inclusion criteria: | 1. Patients with DES implanted, then treated with clopidogrel plus aspirin for 12 months |
2. Informed, written consent from the patient | |
Exclusion criteria: | 1. Age <18 years |
2. Oral anticoagulation therapy | |
3. Drug-eluting stent in an unprotected left main coronary artery | |
4. Contemporaneous enrollment in a different clinical trial | |
5. Malignancies or other comorbid conditions with a life expectancy <2 years | |
6. Known allergy or intolerance to the study medications: aspirin and/or clopidogrel | |
7. Other revascularization with a DES within nine months prior to this study | |
8. Other revascularization with a BMS within four weeks prior to this study |