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临床试验/NCT04121949
NCT04121949已完成不适用

A Prospective, Randomized, Controlled, Parallel-group, Multicentre Trial to Examine the Cost-effectiveness and Safety of Adding the CADScorSystem as a Rule-out Test in Patients Referred With Symptoms Suggestive of Stable Coronary Artery Disease.

Bispebjerg Hospital12 个研究点 分布在 2 个国家目标入组 2,016 人开始时间: 2019年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
2,016
试验地点
12
主要终点
Cumulative number of non-invasive and invasive diagnostic procedures

研究概览

简要总结

This study evaluates the addition of the CADScorSystem to a standard Diamond-Forrester score guided rule-out strategy in ambulatory patients referred with symptoms suggestive of stable coronary artery disease. Half of the patients will undergo stratification using a Diamond-Forrester score only, while the other half will undergo stratification using a Diamond-Forrester score and a CAD-score. The study hypothesis is that the addition of a CAD-score will reduce unnecessary testing without compromising patient safety.

详细描述

Purpose and Rationale for the Study:

The declining incidence of obstructive CAD and a good prognosis for patients with stable angina challenges the resource demanding approach recommended in current guidelines. The CADScor®System may be an efficient, fast and low-cost diagnostic tool with a high rule-out efficiency. The current study aims to investigate if the CADScor®System can be added as a rule-out test in patients referred with suspected stable CAD to reduce unnecessary testing

Study Hypothesis:

A Diamond-Forrester score plus CAD-score guided rule-out strategy is superior to a Diamond-Forrester score guided strategy alone in reducing diagnostic procedures and non-inferior in terms of safety outcomes in patients with symptoms suggestive of stable coronary artery disease.

Study Setting:

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
Single (Outcomes Assessor)

盲法说明

Allocation will be hidden from the independent Clinical Events Committee.

入排标准

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

入选标准

  • Have signed the informed consent form.
  • Males and females, aged 30 years or above.
  • Be able and willing to comply with the clinical investigational plan.
  • Symptoms suggestive of stable coronary artery disease.
  • No history of coronary artery disease (prior myocardial infarction, percutaneous coronary intervention or coronary artery bypass graft).

排除标准

  • Diamond-Forrester score >85%.
  • Prior non-invasive testing for stable CAD or invasive coronary angiography within 6 months of randomization.
  • Implanted donor heart, mechanical heart, mechanical heart pump.
  • Pacemaker or Cardioverter Defibrillator (ICD).
  • Implanted electronic equipment in the area above and around the heart.
  • Significant operation scars, abnormal body shape, fragile or compromised skin in the fourth left intercostal space recording area.
  • Receiving same day treatment with nitro-glycerine on the day of randomization.
  • The exclusion criteria '
  • Diamond-Forrester score >85%' was removed after updating the study according to the 2019 ESC guidelines on chronic coronary syndrome. According to these current guidelines, no patients should be referred to invasive diagnostic test based on their PTP alone, and therefore is this exclusion criteria is no longer relevant.

结局指标

主要结局

Cumulative number of non-invasive and invasive diagnostic procedures

时间窗: 1 year

Difference between the two treatment groups in cumulative number of non-invasive and invasive diagnostic procedures. Non-invasive procedures include exercise electrocardiogram (ECG), cardiac computed tomography angiography (CCTA), Rubidium cardiac PET (Rb-PET), myocardial perfusion imaging (MPI), cardiac magnetic resonance imaging (CMRi) and stress echocardiography. Invasive procedures include invasive coronary angiography (ICA) only.

次要结局

  • Incidence of Major adverse cardiac events (MACE)(1 year)

研究者

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

Eva Prescott

Professor

University Hospital Bispebjerg and Frederiksberg

研究点 (12)

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