跳至主要内容
临床试验/NCT05006183
NCT05006183招募中不适用

Characterization of Coronary Artery Hemodynamic Measurements and Virtual Angioplasty Planning by Instantaneous Wave-free Ratio (iFR) in Multivessel Acute Coronary Syndrome Patients With Evaluation of the Impact on Clinical Outcomes.

Daugavpils Regional Hospital2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2019年8月8日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
150
试验地点
2
主要终点
PCI-related Major adverse cardiac events (MACE)

研究概览

简要总结

A single-center, prospective, randomized, open-label, blinded end-point clinical trial of instantaneous wave-free ratio (iFR) guidance strategy impact on clinical outcomes in multivessel acute coronary syndrome (ACS) patients.

详细描述

The "all-comers" study population consists of hemodynamically stable de novo ACS patients with a stenosis of 50% and more by visual estimation in at least two separate coronary arteries with Thrombolysis in Myocardial Infarction (TIMI) flow ≥ 2 and willing to sign a patient informed consent. ACS diagnosis established by angina pectoris symptoms and/or ECG changes and/or hs-troponin I levels. The use of drug-eluting stents is mandatory in both treatment groups. In the intervention strategy group, patients are treated by the iFR-guided percutaneous coronary intervention (PCI) in one stage. In the control group, patients are treated in accordance with the standard practice of angiography-guided staged approach.

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, Outcomes Assessor)

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 of age and older
  • willing to give informed consent
  • hemodynamically stable de novo acute coronary syndrome patients with a stenosis of 50% and more by visual estimation in at least two separate coronary arteries
  • adequate coronary flow, Thrombolysis in Myocardial Infarction (TIMI) flow ≥ 2
  • sinus rhythm

排除标准

  • inability to give consent;
  • younger than 18 years of age
  • atrial fibrillation rhythm at the time of inclusion
  • with significant valve disease
  • in cardiogenic shock
  • with reduced kidney function - eGFR < 30 (mL/min/1.73m2);
  • with congenital heart defects
  • with acute pulmonary artery embolism;
  • with isolated left main ostial stenosis;
  • on active oncologic treatment or toxic cardiomyopathy;
  • revascularization by PCI is not possible due to other comorbidities or patient denial of treatment.

结局指标

主要结局

PCI-related Major adverse cardiac events (MACE)

时间窗: 12 months

Composite of cardiac death, non-fatal myocardial infarction, unplanned revascularization, stent thrombosis, flow limiting coronary dissections, no-reflow phenomenon, coronary perforations, coronary distal embolization, vascular access site complications requiring blood transfusion or surgical intervention and contrast-induced nephropathy requiring hospitalisation.

次要结局

  • Segmental myocardial deformation by speckle-tracking echocardiography(Index admission, 3 months and 12 months)
  • Health-related Quality of Life(Index admission, 3 months and 12 months)
  • Number of Participants with Decline of eGFR(Index admission, 3 months and 12 months)

研究者

发起方
Daugavpils Regional Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Deniss Vasiljevs

Principal Investigator

Daugavpils Regional Hospital

研究点 (2)

Loading locations...

相似试验