EUCTR2006-000357-22-DE进行中（未招募）不适用
ASSESSMENT OF GLOBAL AND REGIONAL LEFT VENTRICULAR FUNCTION AT REST AND DURING DOBUTAMINE STRESS WITH SONOVUE®-ENHANCED REALTIME 3D-ECHOCARDIOGRAPHY
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 100
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
- •- Availability of results from a pre-study cath-lab examination (cine-ventriculography and coronary angiography) performed within 7 days before planned stress-echocardiography
- •- Given indication for dobutamine stress-echocardiography
- •- Given written Informed Consent to participate in the study.
- •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
- •- Age < 18 years
- •- Pregnant or lactating woman
- •- Known allergy against any of the ingredients of SonoVue®
- •- Unstable cardiac condition according to the contraindications for SonoVue® (cf. SPC)
- •- Any contraindication to dobutamine stress-echocardiography and/or cardiac MRI
- •- Insufficient acoustic window for adequate echocardiographic examination
- •- Participation in another clinical study with an investigational drug (up to 30 days before inclusion).
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