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
相关药物
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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