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临床试验/NCT02014090
NCT02014090已完成不适用

Acute Cardiovascular Effects of External Counterpulsation (ECP) in Comparison With Physical Exercise in Healthy Individuals

Insel Gruppe AG, University Hospital Bern2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2008年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2
主要终点
Myocardial Blood Flow (MBF) measurement by Myocardial Contrast Echocardiography (MCE)

研究概览

简要总结

The purpose of this study in humans with stable coronary artery disease (CAD) treatable by percutaneous intervention (PCI) is to evaluate the efficacy of Enhanced External Counterpulsation (EECP) with regard to coronary collateral growth.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 years, written informed consent to participate in the study

排除标准

  • Pregnancy (serum β-HCG<2 IU/l for all female volunteers)
  • Baseline History:
  • Endurance exercise 5 days before and the days between the exams
  • History of cardiovascular disease or surgery, including arterial hypertension, Raynaud phenomenon, recurrent migraine, or any cardiac rhythm disorder
  • History of metabolic disorder, particularly diabetes mellitus
  • History of respiratory, renal, hepatic or cerebral disease
  • Allergic reactions to Luminity or its components
  • Cardiovascular medication
  • Illness characterized by acute phase response
  • Anaemia with haemoglobin levels < 110 g/L
  • Baseline Physical Examination:
  • Peripheral artery disease
  • Baseline Echocardiogram:
  • Valvular heart disease
  • Aortic aneurysm (any abnormality of ascending aorta, aortic arch or descending aorta)
  • Intra- or extracardiac shunt
  • Systolic or diastolic left ventricular (LV) dysfunction
  • LV-hypertrophy
  • Pulmonary arterial hypertension

结局指标

主要结局

Myocardial Blood Flow (MBF) measurement by Myocardial Contrast Echocardiography (MCE)

时间窗: During ECP respectively Bicycle Exercise, expected to be on average 90 minutes

次要结局

  • Puls Wave Velocity Analysis(At baseline & post intervention, expected to be on average 90 minutes)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Christian Seiler

Prof Dr med

Insel Gruppe AG, University Hospital Bern

研究点 (2)

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