KCT0003063
Terminated
未知
Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-VII: Sirolimus-eluting (Ultimaster) vs. Everolimus-Eluting Stents (Xience)
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Asan Medical Center
- Enrollment
- 400
- Status
- Terminated
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •The patient must be at least 19 years of age.
- •Significant native coronary artery stenosis (\>50% by visual estimate) with lesion length of more than 25mm, which requiring at long stent placement without intervening normal segment.
- •Patients with silent ischemia, stable or unstable angina pectoris, ad Non\-ST\-elevation myocardial infarction (NSTEMI)
- •The patient or guardian agrees to the study protocol and the schedule of clinical and angiographic follow\-up, and provides informed, written consent, as approved by the appropriate Institutional Review Board/Ethical Committee of the respective clinical site.
Exclusion Criteria
- •Any contraindication to any of the following medications: aspirin, heparin, clopidogrel, stainless steel, contrast agents, sirolimus, or everolimus
- •An elective surgical procedure is planned that would necessitate interruption of antiplatelet drugs during the first 6 months post enrollment.
- •Acute ST\-segment\-elevation MI or cardiogenic shock
- •Terminal illness with life expectancy \<1 year
- •In\-stent restenosis at target vessel (either bare metal stent or drug\-eluting stent segment). However, non\-target vessel ISR is permitted.
- •Patients with EF\<30%.
- •Serum creatinine level \= 2\.0mg/dL or dependence on dialysis.
- •Patients with left main stem stenosis (\>50% by visual estimate)
Outcomes
Primary Outcomes
Not specified
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