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临床试验/NCT05658250
NCT05658250进行中(未招募)不适用

Feasibility of CRE8 Polymer-free Amphilimus-eluting sTEnt in Patients With Diffuse Long Lesions (CREATE Trial): Prospective, Observational Study

Yonsei University1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2021年8月3日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
300
试验地点
1
主要终点
Target lesion failure including deaht, MI, ST, TLR

研究概览

简要总结

Observation of the safety and effectiveness of Cre8 stent, Cre8 evo stent in patients with ischemic heart disease with long coronary lesions

详细描述

The purpose of this study is to observe the prognosis of 300 patients with long lesions over 30 mm treated with a new-generation Cre8 stent, Cre8 evo stent that is polymer-free and releases fat-soluble ampilimus in the real world. In addition, in the case of inserting a 46mm very long stent through sub-analysis, we also want to check whether stent expansion is performed through OCT rather than IVUS.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
19 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 19 years of age or older
  • Clinical evidence of coronary artery disease, including asymptomatic ischemia, stable angina, and acute coronary syndrome (unstable angina, non-ST-segment elevation myocardial infarction, ST-segment elevation myocardial infarction)
  • Coronary artery lesion length 30 mm or more
  • Those who voluntarily agreed in writing to participate in this clinical study

排除标准

  • Remaining life expectancy is less than 1 year
  • Subjects with known hypersensitivity or contraindication to the following drugs or substances: heparin, aspirin, clopidogrel, prasugrel, ticagrelor
  • In case the other researcher judges that it is inappropriate to participate in this study (pregnant women, the elderly, etc.)

结局指标

主要结局

Target lesion failure including deaht, MI, ST, TLR

时间窗: 12 months after the index procedure

number of Target lesion failure including deaht, MI, ST, TLR

次要结局

  • All cause death(12 months after the index procedure)
  • Cardiac death(12 months after the index procedure)
  • Myocardial infarction(12 months after the index procedure)
  • Target lesion revascularization(12 months after the index procedure)
  • Stroke(12 months after the index procedure)
  • Stent thrombosis : definite or probable stent thrombosis by ARC definition(12 months after the index procedure)
  • Target vessel revascularization(12 months after the index procedure)
  • BARC bleeding 2-5(12 months after the index procedure)
  • Stent overexpansion by OCT(immediately after the index procedure in hospitalization)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Deok-Kyu Cho

Professor

Yonsei University

研究点 (1)

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