Subjects requiring coronary revascularization with Drug Eluting Stents (DES) coronary revascularization Drug Eluting Stents (DES) The Limus Eluting Orsiro Stent
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: - 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 12 months Event of cardiac death, Myocardial Infarction (MI), Coronary Artery Bypass Graft (CABG), clinically | — |
Secondary
| Measure | Time frame |
|---|---|
| TLF at 6 months follow up 6 months Clinically driven Target Lesion Revascularization (TLR),Target Vessel Revascularization (TVR) 6 months and 12 months event of Vessel Revascularization ,Target Lesion Revascularization (TLR) at 6 and 12 months Event of lesion revascularization,Stent Thrombosis at 6 and 12 months event Stent Thrombosis ,Clinical Device Success Day 0 number of Clinical Device Success,Clinical Procedural Success Day 0 number of Clinical Procedural Success | — |
Countries
Thailand
Contacts
Faculty of Medicine, Chiang Mai University