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临床试验/NCT01091350
NCT01091350已完成不适用

Influence of Equilibration Rate Constant (ke0) of Propofol on the Effect-site Concentration for Loss of Consciousness

Seoul National University Hospital0 个研究点目标入组 60 人开始时间: 2009年5月1日最近更新:
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
60
主要终点
Estimated effect-site propofol concentration at loss of consciousness

研究概览

简要总结

The aim of this study is to validate that an effect compartment concentration for loss of consciousness (LOC) was varied according to different Keo value.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single (Participant)

入排标准

年龄范围
20 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Adult patients undergoing general anesthesia

排除标准

  • •Hepatic or renal disease
  • •Drug addiction

研究组 & 干预措施

Diprifusor group

Active Comparator

Propofol was infused via Diprifusor TCI (Target-controlled infusion)

干预措施: Diprifusor (Target-controlled infusion) (Device)

Orchestra group

Experimental

Propofol was infused via Orchestra TCI

干预措施: Orchestra (Target-controlled infusion) (Device)

结局指标

主要结局

Estimated effect-site propofol concentration at loss of consciousness

时间窗: after propofol infusion

次要结局

  • Time to loss of consciousness(after propofol infusion)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jung-Won Hwang

MD

Seoul National University Hospital

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