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临床试验/NCT05209503
NCT05209503Unknown不适用

Prognostic Implications of AccuFFRangio-based Functional Evaluation for Guiding Coronary Intervention for Non-IRA Stenosis in Patients With STEMI

Wuhan Asia Heart Hospital0 个研究点目标入组 500 人开始时间: 2022年2月15日最近更新:
适应症

试验速览

阶段
不适用
入组人数
500
主要终点
Vessel-oriented composite endpoints (VOCEs)

研究概览

简要总结

This is a prospective, single-center clinical trial. AccuFFRangio (ArteryFlow Technology Co., Ltd., Hangzhou, China) is a novel method for evaluating the functional significance of coronary stenosis by computing the pressure in the vessel based on angiographic images. The aim of this study was to evaluate the diagnostic accuracy and prognostic implications of AccuFFRangio in patients with ST-segment elevation myocardial infarction (STEMI).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • 18 Years and older
  • STEMI patients with primary percutaneous coronary intervention within 24 hours with at least 1 non-IRA
  • Diameter stenosis of 50%-90% by visual estimate
  • Reference vessel size > 2 mm in stenotic segment by visual estimate

排除标准

  • LVEF ≤ 40%
  • eGFR < 60 mL/min
  • Allergy to contrast media, adenosine
  • Prior CABG

结局指标

主要结局

Vessel-oriented composite endpoints (VOCEs)

时间窗: 1 year

Composite of vessel-related cardiovascular death, vessel-related myocardial infarction, and ischemia-driven target vessel revascularization.

Post-PCI AccuFFRangio

时间窗: 1 year

AccuFFRangio limits to yield no VOCEs (Composite of vessel-related cardiovascular death, vessel-related myocardial).

次要结局

  • Cost analysis(1 year)
  • Prognostic implications(1 year)

研究者

申办方类型
Other
责任方
Sponsor

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