NCT01055210已完成不适用
Optimisation of Cardiac Resynchronisation Therapy by Non-invasive Cardiac Output - The CHOICE2 Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 31
- 试验地点
- 1
- 主要终点
- 6 minute hall walk test
研究概览
简要总结
An evaluation of the role of resting and exercise cardiac output measurement, by the inert gas rebreathing method, in optimisation of patients with cardiac resynchronisation pacemakers.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 100 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Cardiac Resynchronization Device in situ for Heart Failure
排除标准
- •Unable to cope with mouthpiece
- •Estimated life expectancy < 6 months
结局指标
主要结局
6 minute hall walk test
时间窗: 4 months
次要结局
- Echocardiographic measures of desynchrony(3 months)
研究者
研究点 (1)
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