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临床试验/EUCTR2008-004895-39-GB
EUCTR2008-004895-39-GB进行中(未招募)不适用

Quantitative Assessment of Myocardial Perfusion with Magnetic Resonance Using an Intravascular Contrast Agent

King's College London0 个研究点开始时间: 2008年10月31日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)

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

  • Patients referred for MR adenosine stress perfusion, with or without known coronary artery disease, with or without prior myocardial revascularization
  • The subject is =18 years of age
  • The subject is conscious and able to comply with the study procedures
  • Written informed consent has been obtained
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Contraindications for MRI
  • Contraindications to Gadolinium based contrast agents (known allergies or a contra indication to Gd
  • chelates or renal insufficiency)
  • Contraindications to Adenosine stress
  • Myocardial infarction <3 days
  • Unstable angina pectoris
  • Severe arterial hypertension
  • Asthma or severe obstructive pulmonary disease requiring treatment (chronic obstructive pulmonary disease COPD)
  • Sick sinus syndrome or a symptomatic bradycardia, AV block >IIa, trifascicular block
  • Allergy against vasodilator
  • Allergy against Gadolinium based contrast agents or renal insufficiency
  • Other contraindications for adenosine or dipyridamole administration
  • Heart failure (NYHA IV)
  • The subject’s ECG shows prolonged QT interval
  • Severe arterial hypotension (< 90 mmHg systolic)
  • Claustrophobia

研究者

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