跳至主要内容
临床试验/NL-OMON54357
NL-OMON54357招募中不适用

Addition of FFRct in the diagnostic pathway of patients with stable chest pain to reduce unnecessary invasive coronary angiography - FUSION Study

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 528 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
528

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Age >= 18 years
  • - Stable chest pain and the patient underwent CCTA which demonstrated >=*50% but
  • less than 90% stenosis in any major epicardial vessel with a diameter >= 2 mm.

排除标准

  • - Inability to provide informed consent
  • - Unstable angina according to ESC guidelines
  • - Unstable clinical status
  • - Expected inability to complete follow-up and comply with follow-up aspects of
  • the protocol
  • - History of coronary revascularisation
  • - Non-invasive or invasive diagnostic testing for CAD within the past 12 months
  • (with the exception of exercise ECG)
  • - Unsuitable for revascularisation if required (for example due to
  • comorbidities or anatomical features)
  • - Poor CT quality with expected inability to perform FFRct analysis

研究者

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