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 Xience Xpedition™/Alpine™, Everolimus-eluting Stent for Coronary Atherosclerotic Lesions: HOST-Alpine Registry
The objectives of this study are
1. To establish a prospective registry of the whole patients who received percutaneous
coronary intervention with Xience Xpedition™/Alpine™ stent
2. To evaulate the long-term efficacy and safety of coronary stenting with the Xience
Xpedition™/Alpine™ stent
3. To compare the long-term efficacy and safety of coronary stenting between the Xience
Xpedition™/Alpine ™ stent and other contemporary drug-eluting stents which had
established their own registry
Secondary endpoints of this study are
Stent thrombosis-24 hours(acute), 30 days(subacute), 1 year(late), every 1 year till 3
years(very-late) after index PCI
Target vessl failure
Composite rate of cardiac death and any MI, 3 years
Composite rate of all death and any MI
Composite rate of all death, any MI, and any repeat revascularization
Compliance and therapy interruptions with prescribed adjunctive antiplatelet therapy
;
Observational Model: Case-Only, Time Perspective: Prospective
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