NCT02932371终止不适用
Evaluation of the ECOM™ Monitor for Continuous and Non-invasive Measure of the Cardiac Output in Cardiac Surgery Patients
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- Hopital Foch
- 入组人数
- 5
- 试验地点
- 4
- 主要终点
- Cardiac output
研究概览
简要总结
The objective of the study is to estimate the reliability of the determination of the cardiac output measured by the ECOM™ device. This study will be performed with the latest version of the software which should give better results than those published previously. Two techniques of measure of the cardiac output will be compared: the reference measure by trans-esophageal echography and the bioimpedance used by the ECOM™. monitor.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 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
- 否
入选标准
- •Patients over18 years
- •Needed cardiac surgery,
- •Needed a monitoring by transesophageal ultrasound ,
- •Benefiting from a social security scheme
- •Having given their written consent.
排除标准
- •Pregnant or breast-feeding women,
- •Allergy to polyvinylchloride (PVC),
- •The patients for whom a difficulty of ventilation with a mask or intubation is envisaged,
- •Contraindication to transesophageal ultrasound, a steady cardiac arrhythmia, a flight or an aortic shrinkage.
结局指标
主要结局
Cardiac output
时间窗: 4 hours
次要结局
未报告次要终点
研究者
研究点 (4)
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