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临床试验/NCT02590926
NCT02590926已完成不适用

Safety of Negative FrActional Flow Reserve in Patients With ChallEnging Lesions

A.O.U. Città della Salute e della Scienza1 个研究点 分布在 1 个国家目标入组 285 人开始时间: 2014年9月26日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
285
试验地点
1
主要终点
MACE

研究概览

简要总结

Fractional Flow Reserve (FFR) has recently emerged and has been largely validated as a safe and efficacious way of ischemia testing for patients with stable angina. The new recently ESC guidelines have strongly suggested a FFR based approach for patients with stable angina, also for those with challenging lesions like left main disease, severe multivessel stenosis for heart failure patients and those with single remaining vessels although left main disease and an ejection fraction less than 30% are exclusion criteria of the randomized controlled trials on this topic. Consequently the investigators performed a prospective multicenter study to understand the safety and efficacy of a FFR based approach for these patients.

详细描述

The present is a multicenter prospective study enrolling all patients with stable angina and/or documented ischemia presenting with:

  • An angiographic stenosis of more than 50% and less than 90% of the left main
  • Any proximal descending anterior with a stenosis of more than 50% and less than 90%
  • Two or three vessel disease with a stenosis of more than 50% and less than 90% and a left ventricle ejection fraction less than 40%
  • Single remaining patent coronary artery with stenosis >50% and less than 90%

In all of these patients FFR (Fractional Flow Reserve) will be performed according to guidelines and stenting will be performed or deferred according to the result of this test. Other techniques, like iFR, IVUS and OCT will be left at the operators' choice and will be recorded. MACE (a composite end point of death, myocardial infarction and target vessel revascularization and stent thrombosis) will be the primary end point, while its single components will be the secondary ones.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • An angiographic stenosis of more than 50% and less than 90% of the left main
  • Any proximal descending anterior with a stenosis of more than 50% and less than 90%
  • Two or three vessel disease with a stenosis of more than 50% and less than 90% and a left ventricle ejection fraction less than 40%
  • Single remaining patent coronary artery with stenosis >50% and less than 90%

排除标准

  • Severe aortic stenosis

结局指标

主要结局

MACE

时间窗: 3 years

composite end point of death, myocardial infarctio, target vessel revascularization and target lesion revascularization, stent thrombosis

TVF (only for deferred lesion)

时间窗: 1 and 2 years

composite of cardiac death,myocardial infarction and target vessel revascularization due to deferred lesion

次要结局

  • Death(1 and 2 years)
  • TLR(1 and 2 years)
  • AMI(1 and 2 years)

研究者

发起方
A.O.U. Città della Salute e della Scienza
申办方类型
Other
责任方
Principal Investigator
主要研究者

Claudio Moretti

Head, Cardiology Cath Lab

A.O.U. Città della Salute e della Scienza

研究点 (1)

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