NCT00598936终止不适用
A Prospective Study With a New Device for the Monitoring of Cerebral Oxygenation on Cardiac Surgery Patients
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 21
- 试验地点
- 1
- 主要终点
- To test a new device for Cerebral Oxygenation Monitoring
研究概览
简要总结
The purpose of this study is to determine whether a new cerebral oxygenation monitoring device is comparatively similar to the current approved devices.
详细描述
Cerebral oxygenation monitoring is an innovative way to monitoring cardiac surgery patients intraoperatively to reduce the incidence of postoperative hypoxic side effects. There are a number of approved devices already in the market that have proved their efficacy.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
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
- •To be 18 years old or older
- •Scheduled for cardiac surgery
- •Treatment will include 72 hours or more of hospital stay
- •Understand enough about the risks and benefits of the study to be able to make an informed decision before agreeing to be in the study
排除标准
- •History of cerebrovascular disease
- •History of skin problems on forehead (skin rashes, acne, allergies, etc.)
- •History of craniofacial surgeries
结局指标
主要结局
To test a new device for Cerebral Oxygenation Monitoring
时间窗: 12 hours
次要结局
- Safety of human forehead skin during period of probe adhesion(12 hours)
研究者
研究点 (1)
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