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
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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