NCT01732133已完成不适用
Evaluation of the System NEXFIN for Continuous and Non-invasive Measure of the Blood Pressure During Cesarean Delivery Practised Under Spinal Anesthesia
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Hopital Foch
- 入组人数
- 171
- 试验地点
- 2
- 主要终点
- Comparison between Nexfin and intermittent measurements of blood pressure
研究概览
简要总结
Hypotension after spinal anesthesia for cesarean delivery occurs frequently. Oscillometric measurement gives intermittent informations. Nexfin, a continuous noninvasive device, could help to detect hypotension.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •adult patients undergoing elective cesarean delivery performed under spinal anesthesia
排除标准
- •patients with a heart rhythm disorder, Raynaud's disease or a history of vascular surgery of the upper limb
研究组 & 干预措施
Measurement of arterial pressure
Experimental
干预措施: Nexfin (Device)
结局指标
主要结局
Comparison between Nexfin and intermittent measurements of blood pressure
时间窗: two years
Bland and Altman analysis (bias and limits of agreement). Analysis concerns data from intrathecal injection to childbirth
次要结局
- Area under the curve between both measurements(two years)
研究者
研究点 (2)
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