跳至主要内容
临床试验/NCT05824520
NCT05824520
招募中
不适用

Coronary Computed Tomography-Derived Fraction Flow Reserve (FFR)-Guided Invasive Treatment Strategy (ITS) Versus Optimal Medical Therapy (OMT) Alone in Patient With Chronic Coronary Syndrome

Second Affiliated Hospital, School of Medicine, Zhejiang University1 个研究点 分布在 1 个国家目标入组 1,066 人2024年10月10日

概览

阶段
不适用
干预措施
ITS plus OMT
疾病 / 适应症
Coronary Artery Disease
发起方
Second Affiliated Hospital, School of Medicine, Zhejiang University
入组人数
1066
试验地点
1
主要终点
Major adverse cardiac events (MACE)
状态
招募中
最后更新
2个月前

概览

简要总结

The overall purpose of ACCURATE II trial is to compare the clinical outcomes of CT-derived FFR guided strategy versus medical therapy in patients with chronic coronary syndrome.

详细描述

ACCURATE II is a prospective, multicenter, randomized clinical trial comparing the clinical outcome and cost-effectiveness of the two management strategies. CT-FFR-guided invasive treatment strategy versus optimal medical therapy, in management of patients with chronic coronary syndrome. The study is powered to detect if the primary endpoint by the CT-FFR-guided strategy is superior to the medical therapy strategy.

注册库
clinicaltrials.gov
开始日期
2024年10月10日
结束日期
2032年10月20日
最后更新
2个月前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

发起方
Second Affiliated Hospital, School of Medicine, Zhejiang University
责任方
Sponsor

入排标准

入选标准

  • Age ≥ 18 years, with at least one vessel has CT-derived FFR≤0.80
  • Patients with chronic coronary syndromes
  • Signed written informed consent

排除标准

  • The patient has a known hypersensitivity or contraindication to any of the following medications: Heparin, Aspirin, Clopidogrel, Prasugrel, Ticagrelor, Contrast media (Patients with documented sensitivity to contrast media which can be effectively pre-medicated with steroids and diphenhydramine \[e.g. rash\] may be enrolled)
  • Prior percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG)
  • Sinus arrhythmia, cardiogenic shock, or severe heart failure (NYHA≥III)
  • Inability or unwillingness to undergo CT scan or coronary angiography
  • Patients on hemodialysis or with severe hepatic or renal insufficiency
  • Left main coronary artery stenosis ≥ 50%
  • Target vessel total occlusion
  • Pregnancy or intention to become pregnant during the course of the trial
  • Patients with a life expectancy less than 2 years

研究组 & 干预措施

CT-derived FFR guided-ITS group

CT-derived FFR≤0.8; ITS plus OMT

干预措施: ITS plus OMT

Medical therapy group

CT-derived FFR≤0.8; OMT alone

干预措施: OMT

结局指标

主要结局

Major adverse cardiac events (MACE)

时间窗: 1 year

A composite of all-cause death, myocardial infarction (MI) or ischemia-driven revascularization.

次要结局

  • Death(1 year)
  • Revascularization(1 year)
  • MACE(1 month, 2 years, 3 years, 5 years)
  • Cost-effectiveness analysis(1 year)
  • MI(1 year)
  • Stroke(1 year)
  • Quality of life assessed by Seattle Angina Questionnaire(1 year)

研究点 (1)

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