跳至主要内容
临床试验/NCT03661827
NCT03661827已完成不适用

Diagnostic Accuracy in Left Ventricular Systolic Dysfunction for Identifying Coronary Artery Disease With Dobutamine Versus Adenosine Non-invasive Stress Cardiac Magnetic Resonance Evaluation

University of Leicester1 个研究点 分布在 1 个国家目标入组 69 人开始时间: 2019年2月5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
入组人数
69
试验地点
1
主要终点
Presence of severe CAD (stenosis >70%) on invasive angiography and will be assessed on a per vessel basis

研究概览

简要总结

This is a single centre, prospective diagnostic accuracy study to assess the comparative sensitivity of dobutamine versus adenosine for detection of severe non-infarct epicardial coronary artery stenosis in subjects with reduced LV EF ( EFed referred for clinical coronary angiography for investigation of symptoms or to establish the cause heart failure. Study participants will be identified from hospital angiography referral waiting lists, or already known with CAD and from heart failure outpatient clinics at Glenfield General Hospital. Clinical and CMR data will be collated on-site (at Glenfield General Hospital) from medical records stored and stress cardiac MRI scans at Glenfield General Hospital. The analysis will occur over a 12-month period following study commencement.

详细描述

Aim The primary aim of this study is to assess the comparative sensitivity of adenosine and dobutamine for detection of severe CAD in patients with HFrEF. Secondary aims are to evaluate how the addition of stress perfusion may alter management compared to CMR without stress.

Primary hypothesis:

In patients with HFrEF (EF≤40%), dobutamine perfusion has superior sensitivity to adenosine for the detection of non-infarct severe CAD (>70% epicardial coronary artery stenosis).

Secondary hypotheses The addition of stress perfusion imaging to CMR cine and LGE imaging does not significantly increase the accuracy for determining whether the aetiology of HFrEF is due to CAD or not.

The response to adenosine (haemodynamics/splenic T1) will be inversely related to markers of LV dysfunction/injury (high sensitivity troponin I/B-type natriuretic peptide) and directly to EF.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

盲法说明

yES

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •- HFrEF (LV EF≤40%, based on either echocardiography, CMR or nuclear perfusion imaging) consistent with recent guidelines for diagnosis of HFrEF [38] referred for investigation of CAD.
  • •2. Age ≥18 years ≤90 years old
  • •Understand written and verbal English.
  • •Patients are not involved in other research studies within the last year.

排除标准

  • •Absolute contraindication to MRI.
  • •Absolute contraindication to dobutamine OR adenosine;
  • •Stage III-V renal disease (estimated glomerular filtration rate <30ml/min/1.73m
  • •4. Previous coronary artery bypass grafting.
  • •Unstable angina or MI within 6 weeks.
  • •Persistent atrial fibrillation
  • •Participants who are involved in current research or have recently been involved in any research prior to recruitment
  • •Participants who don't speak or understand verbal or written English

研究组 & 干预措施

Patients with heart failure

Experimental

Patients with heart failure

干预措施: Stress Cardiac MRI (Diagnostic Test)

结局指标

主要结局

Presence of severe CAD (stenosis >70%) on invasive angiography and will be assessed on a per vessel basis

时间窗: 2 years

if positive

次要结局

  • Presence of inducible wall motion abnormality as a response to dobutamine by Cardiac MRI(2 years)
  • Haemodynamic/splenic T1 mapping value in (ms) to adenosine by cardiac MRI scan.(2 years)
  • Myocardial perfusion reserve (ml/min/g) by cardiac MRI scan.(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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