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临床试验/KCT0000464
KCT0000464已完成未知

Efficacy of Bispectral Monitoring for Propofol and Midazolam induced Sedation During Colonoscopy

Hanyang University Seoul Hospital0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
18(Year) 至 o Limit(—)
性别
All

入选标准

  • Healthy adult

排除标准

  • Excluded from the study were patients with ASA status III or higher, those who refused sedation during colonoscopy, who were hospitalized, and who were pregnant or lactating, as well as patients with an allergy to eggs, beans or latex, with a previous history of alcohol or sedative overdose and adverse events associated with propofol, with sleep apnea or acute gastrointestinal hemorrhage and with a recent history of central nervous system (CNS) abnormalities (e.g. stroke).

研究者

发起方
Hanyang University Seoul Hospital

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