NCT01567371已完成不适用
Use of the LiDCORapid Monitor in Patients During Graded Phlebotomy and the Removal of Autologous Blood
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Difference in Pulse Pressure Variability From Baseline to Post-ANH
研究概览
简要总结
This is a study to validate the utility and accuracy of the non-invasive device (LiDCOrapid monitor) during a period of phlebotomy and graded blood loss in patients who are having cardiac surgery.
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
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients scheduled for intraoperative phlebotomy following anesthetic induction to obtain autologous blood for use following cardiopulmonary bypass and cardiac surgery.
排除标准
- 未提供
研究组 & 干预措施
LiDCO rapid monitor
Experimental
干预措施: LiDCO rapid monitor (Device)
结局指标
主要结局
Difference in Pulse Pressure Variability From Baseline to Post-ANH
时间窗: 1 Day
The difference in pulse pressure variability during a period of phlebotomy and graded blood loss, measured before phlebotomy or acute normovolemic hemodilution (ANH) and immediately after.
次要结局
- Difference in Stroke Volume Variability From Baseline to Post ANH.(1 Day)
研究者
Joseph D. Tobias
Chairman, Dept. of Anesthesiology & Pain Medicine
Nationwide Children's Hospital
研究点 (1)
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