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临床试验/NCT04970082
NCT04970082已完成不适用

A Randomized Crossover Study to Evaluate and Compare the Reproducibility and Tolerability of Direct Wire Pacing for Measuring Fractional Flow Reserve Versus Standard Method in Subjects With FFR Indications

Centre Recherche Cardio Vasculaire Alpes1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2021年6月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
150
试验地点
1
主要终点
Reproducibility of the FFR measurement

研究概览

简要总结

This is a randomized, non-inferiority, crossover investigation comparing the Direct Wire Pacing (DWP) versus standard method to measure Fractional Flow Reserve (FFR) in subjects with FFR indications.

All subjects requiring on a clinical basis a pressure wire assessment of coronary artery stenosis(es) will be eligible to take part in the study.

详细描述

Pressure wire-based Fractional Flow Reserve (FFR) has become the reference standard index of haemodynamic significance to guide revascularisation of intermediate coronary artery lesions.

The FFR measurement determines the ratio of the maximum blood flow that can be achieved in a diseased or narrowed coronary artery to the maximum blood flow in a normal coronary artery. This ratio represents the potential decrease in distal coronary flow relative to coronary stenosis.

FFR is easily measured during routine coronary angiography using a pressure wire to calculate the ratio of coronary pressure distal to a stenosis or diseased segment to aortic pressure under conditions of maximum myocardial hyperemia. An FFR of 1.0 is widely accepted as normal. An FFR of less than 0.80 is generally considered to be associated with coronary ischemia and widely accepted in favor of revascularization rather than conservative management.

The current standard method of measuring FFR is to insert a pressure wire into the coronary artery while the hyperaemic agent, usually adenosine, is delivered by intracoronary bolus or continuous intravenous injection.

Administration of adenosine may cause bradycardia and thus cause patient vagal discomfort. Direct Wire Pacing (DWP) can potentially overcome the drawbacks of the standard method when measuring FFR. Indeed, DWP allows to transmit an electrical current from the external pacemaker to the heart thanks to metallic FFR guidewire already used, and thus prevent bradycardia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Diagnostic
盲法
Single (Participant)

入排标准

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

入选标准

  • •Eligible patient for coronary angiography.
  • •Inclusion Criteria:
  • •The patients included in the study must meet the following inclusion criteria :
  • •Patients ≥ 18 years old
  • •Patients with FFR indications
  • •Has given consent to undergo diagnostic coronary procedure
  • •Patients able to understand and provide informed consent
  • •Patients with Social Security coverage
  • •Prior to randomisation: Angiography demonstrates at least one coronary stenosis in an artery, requiring FFR measurement for physiological assessment.

排除标准

  • •The patients included in the study should not meet the following inclusion criteria :
  • •Contraindications to use sensitivity to Adenosine or any of its excipients
  • •Technically inaccessible stenosis(es)
  • •Pregnant or breastfeeding woman
  • •Patients under judicial protection, tutorship or curatorship
  • •Patient participating in another interventional clinical trial

研究组 & 干预措施

FFR followed by FFR-DWP (investigation)

Experimental

The FFR measurement is performed with the standard method first followed by the FFR measurement with the DWP method.

干预措施: FFR DWP (Diagnostic Test)

FFR followed by FFR-DWP (investigation)

Experimental

The FFR measurement is performed with the standard method first followed by the FFR measurement with the DWP method.

干预措施: FFR (Diagnostic Test)

FFR-DWP (investigation) followed by FFR

Experimental

The FFR measurement is performed with the DWP method first followed by the FFR measurement with the standard method.

干预措施: FFR DWP (Diagnostic Test)

FFR-DWP (investigation) followed by FFR

Experimental

The FFR measurement is performed with the DWP method first followed by the FFR measurement with the standard method.

干预措施: FFR (Diagnostic Test)

结局指标

主要结局

Reproducibility of the FFR measurement

时间窗: Intraoperative

Evaluated by the number of patients with comparable FFR ratio recording. The FFR ratio should remain constant (+/-0.02) between the two modes of measuring FFR.

次要结局

  • correlation between a disproportionately high FFR value and la presence of a (partially) infarcted territory(Intraoperative)
  • Number of participants with Adverse Events(Intraoperative)
  • Tolerance(Intraoperative)

研究者

发起方
Centre Recherche Cardio Vasculaire Alpes
申办方类型
Other
责任方
Sponsor

研究点 (1)

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