The objective of this study is to evaluate the safety and long-term effectiveness of coronary stenting with the zotarolimus eluting stent (ZES) and to determine clinical device and procedural success during commercial use of ZES. The investigators will compare 2nd generation ZE (Endeavor resolute, active prospective arm) with 1st generation ZES (Endeavor Sprint, retrospective arm).
Study Type
OBSERVATIONAL
Enrollment
4,000
2nd generation ZES
1st generation ZES
Hallym University Sacred Heart Hospital
Anyang, South Korea
NOT_YET_RECRUITINGMajor Adverse Cardiac Events (composite of cardiac death, non-fatal MI, target lesion revascularization)
Time frame: 12 months
In-stent & In-segment Late Loss
Time frame: 9 months
Stent Thrombosis
Time frame: 1 year
Target Vessel Failure (composite of cardiac death, MI, and TVR)
Time frame: 12 months
Any death, cardiac death, MI, TLR, TVR
Time frame: 1 year
Composite rate of cardiac death and any MI
Time frame: 1 year
Composite rate of all death and any MI
Time frame: 1 year
Composite rate of all death, any MI (Q-wave and non Q-wave) and any repeat revascularization
Time frame: 1 year
Compliance and therapy interruptions with prescribed adjunctive antiplatelet therapy
Time frame: 1 year
Clinical device and procedural success
Time frame: During the health care facility stay
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