Coronary Artery Disease Clinical Trial
Official title:
Harmonizing Optimal Strategy for Treatment of Coronary Atherosclerotic Lesions - Registry-based Study on the Effect and Safety of Onyx™, Zotarolimus-eluting Stent for Coronary Atherosclerotic Lesions: HOST-Onyx Registry
The objectives of this study are
1. To establish a prospective registry of the whole patients who received percutaneous
coronary intervention with Resolute Onyx™ stent.
2. To evaluate the long-term efficacy and safety of coronary stenting with the Resolute
Onyx™ stent.
3. To compare the long-term efficacy and safety of coronary stenting between the Resolute
Onyx™ stent and other contemporary drug-eluting stents which had established their own
registry.
Secondary endpoints are
1. Stent thrombosis-24 hours(acute), 30 days(subacute), 1 year(late), every 1 year till 3
years(very-late) after index PCI (percutaneous coronary intervention),
2. Target vessel failure
3. Composite rate of cardiac death and any MI, 3 years
4. Composite rate of all death and any MI
5. Composite rate of all death, any MI, and any repeat revascularization
6. Compliance and therapy interruptions with prescribed adjunctive antiplatelet therapy
7. Clinical device and procedural success
;
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