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Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Symptomatic coronary artery disease Subject signed informed consent for data release Subject is willing to participate at all follow up assessments Subject is 21 years of age
Exclusion criteria
Exclusion criteria: Exclusion Criteria Subject did not sign informed consent for data release Known intolerance to aspirin, clopidogrel, ticlopidine, heparin or any other anticoagulation / antiplatelet therapy required for PCI, stainless steel, Sirolimus or contrast media Planned surgery within 6 months of PCI unless dual antiplatelet therapy will be maintained Pregnancy Currently participating in another study and primary endpoint is not reached yet.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Target Lesion Failure (TLF) at 12 months Composite of cardiac death, target vessel Q-wave or non-Q wave Myocardial Infarction (MI), Emergent | — |
Secondary
| Measure | Time frame |
|---|---|
| Target Lesion Failure (TLF) at 6 months 6 months follow up (FUP) | — |
Contacts
Chulalongkorn University