跳至主要内容
临床试验/EUCTR2013-001225-11-FI
EUCTR2013-001225-11-FI进行中(未招募)不适用

Quantitative myocardial perfusion response to adenosine and regadenoson in patients with suspected coronary artery disease - RegWater

Turku University Hospital0 个研究点目标入组 30 人开始时间: 2013年5月13日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • One of the following:
  • Suspected CAD and referred for cardiac PET perfusion imaging based on clinical indications
  • Known CAD and referred for cardiac PET perfusion imaging based on clinical indications
  • Patients have been or are referred for coronary angiography, either noninvasive or invasive
  • Informed consent from the patient
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 8
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 7

排除标准

  • Continuing, uncontrolled unstable angina symptoms or urgent CABG after invasive coronary angiography
  • ST-elevation myocardial infarction (STEMI)
  • EF < 40% or diagnosis of cardiomyopathy
  • Prior coronary artery bypass grafting (CABG)
  • Haemophilia, Von Willebrand's disease or other coagulation disorder
  • Severe pulmonary disease
  • Symptomatic asthma
  • Severe valvular disease
  • Uncontrolled hypertension (>180/110 mmHg)
  • Moderate to severe renal failure
  • Women with childbearing potential
  • Age < 18 or > 80 years
  • Unstable asthma
  • II or III degree AV block or sick sinus syndrome without pacemaker
  • Severe hypotension (systolic bloodpressure < 90 mmHg),
  • Allergy to x-ray contrast agents (patients have also angiography)

研究者

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