KCT0007397尚未招募未知
Comparison between abluminal biodegradable polymer ultrathin sirolimus-eluting stent and durable-polymer everolimus-eluting stent (GENOSS randomized clinical trial)
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 850
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 19(Year) 至 100(Year)（—）
- 性别
- All
入选标准
- •? 19 years of age or older
- •? Patients diagnosed with stable coronary artery disease or acute coronary syndrome and with more than 50% coronary stenosis requiring stent insertion
- •? A person who can voluntarily sign the consent form
排除标准
- •? If the following drugs are irritable or contraindicated (aspirin, clopidogrel, ticagrelor, prasugrel, heparin, sirolimus, or everolimus)
- •? a pregnant woman
- •? A person who is expected to have a life expectancy of less than one year due to non-heart disease or less compliant with treatment (as determined by medical judgment by the investigator)
- •? Patients who refused to participate in the study
研究者
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