NCT01775306已完成不适用
Not Invasive Monitoring at Cardiac Recompensation
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 49
- 试验地点
- 1
- 主要终点
- suitable Data
研究概览
简要总结
The aim of this study is to find out if data can be provided by external sensor technology which is suitable for controlling the therapy of patients with cardiac recompensation.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 90 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •patients with acute or chronic cardiac decompensation with and without pulmonary oedema
- •male and female patients aged at least 18 years
排除标准
- •pregnancy or breast feeding
- •implanted pacemaker / CRT / ICD exept Medtronic OptiVol
- •patients being unable to consent
结局指标
主要结局
suitable Data
时间窗: 15 minutes per day and per patient, 3-5 days, at most 14 days
次要结局
未报告次要终点
研究者
研究点 (1)
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