跳至主要内容
临床试验/NCT05344612
NCT05344612招募中不适用

Clinical Outcomes and Cost-effectiveness of a Diagnostic and Treatment Strategy of Upfront CTCA Plus Selective Non-invasive Functional Imaging Compared With Standard Care in Patients With Chest Pain and Suspected Coronary Artery Disease

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)2 个研究点 分布在 1 个国家目标入组 6,444 人开始时间: 2022年9月14日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
6,444
试验地点
2
主要终点
Composite of all-cause mortality and non-fatal myocardial infarction

研究概览

简要总结

Rationale:

Patients with chest pain usually undergo multiple diagnostic examinations to demonstrate or rule out atherosclerotic coronary artery disease (CAD). In addition to high healthcare costs, some of the examinations do not assess the presence of CAD, which means that patients may be undertreated and are at risk for myocardial infarction. A uniform diagnostic and treatment strategy that uses computed tomography coronary angiography (CTCA) as initial examination may reduce major adverse cardiac events (MACE) and may reduce healthcare costs. In addition, we hypothesize that this strategy improves angina-related health status and reduces the number of invasive coronary angiograms (CAG's).

Objectives:

  • To show that the intervention is non-inferior to the control with regards to clinical outcomes
  • To show superiority of the intervention with regards to clinical outcomes

Study design: National multicenter prospective randomized controlled trial.

Study population: Patients with suspected stable CAD.

Intervention: upfront CTCA to diagnose CAD and guide optimal medical therapy (OMT). Patients with obstructive CAD and refractory angina despite OMT will undergo non-invasive ischemia imaging to guide revascularization.

Control: Standard of care. Diagnosis and treatment are at the discretion of the attending cardiologist.

Main study end point: Composite of all-cause mortality and non-fatal myocardial infarction.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

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

排除标准

  • Presentation with acute coronary syndrome
  • Acute coronary syndrome within last 3 months
  • History of obstructive coronary artery disease on imaging
  • History of PCI and/or CABG
  • Severe renal failure
  • Severe allergy to ionidated contrast medium
  • Known pregnancy
  • Patients with an estimated life expectancy of less than 1 year

结局指标

主要结局

Composite of all-cause mortality and non-fatal myocardial infarction

时间窗: 1 Year

次要结局

未报告次要终点

研究者

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

J.P.S Henriques

Prof.Dr.

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

研究点 (2)

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