Pragmatic Trial Comparing Symptom-Oriented Versus Routine Stress Testing in High-Risk Patients Undergoing Percutaneous Coronary Intervention

Asan Medical Center0 个研究点目标入组 1,707 人开始时间: 待定最近更新: 2022年11月28日

适应症

试验速览

阶段: 未知
状态: 已完成
发起方: Asan Medical Center
入组人数: 1,707

研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

we found no significant between-group difference in the primary composite outcome of death, myocardial infarction, or hospitalization for unstable angina at 2 years.

研究设计

研究类型: Interventional Study

入排标准

年龄范围: 19(Year) 至 0No Limit（—）
性别: All

入选标准

•Subject was > 19 years of age.
•Subjects who underwent successful PCI with contemporary drug eluting stent or contemporary bioresorbable vascular scaffold.
•Patients must have at least one of the following high-risk clinical, lesion, or procedure-related risk factors.
•3-1. Clinical factors; diabetes, renal insufficiency/failure, enzyme positive acute coronary syndrome (ACS) (STEMI or NSTEMI).
•3-2. Lesion- or procedure-related factors ; left main lesion, bifurcation lesion, ostial lesion, chronic total occlusion lesion, multivessel disease (= 2 vessels stented), restenotic lesion, diffuse long lesion (lesion length =30 mm or stent length =32 mm), or vein bypass graft stented
•The patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate Institutional Review Board/Ethical Committee of the respective clinical site.

排除标准

•Cardiogenic shock at the index admission
•Subject treated with only bare metal stent or balloon angioplasty during the index procedure.
•Pregnant and/or lactating women.
•Concurrent medical condition with a life expectancy of less than 1 years
•Patients who are actively participating in another drug or device investigational study, which have not completed the primary endpoint follow-up period.
•6 Subject was unable to provide written informed consent or participate in long-term follow-up.

研究者

发起方

Asan Medical Center

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