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临床试验/IRCT2016082819470N44
IRCT2016082819470N44已完成2 期

Comparison of depth of anesthesia in induction with sodium thiopental & propofol in elective cesarean section by BIS, IFT

Vice Chancellor for Research, Shiraz University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
no limit 至 no limit(—)
性别
Female

入选标准

  • 90 pregnant women (ASA I- II) who are under general anesthesia for elective cesarean section. Exclusion criteria: Patients who are not properly cooperate; patients who received magnesium sulfate MgSO4 before the study; mental disorders; Patients who have a history of previous awareness during general anesthesia, patients who take blood pressure medication or patients who require the use of vasodilators or vasodepressor drugs; patients who consume human stimulant or psychotropic drugs; mothers with multiple gestation or preterm labor; fetal distress, patients with neuromuscular diseases, opium addicts; history of multiple drug allergies or sensitivity to anesthetics; patients with bradycardia and heart block.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for Research, Shiraz University of Medical Sciences

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