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临床试验/IRCT201112024969N5
IRCT201112024969N5已完成2 期

Comparison of depth of anesthesia in patients under general anesthesia with Propofol or Isofluran undergoing total abdominal hysterectomy with bispectral index

Tehran University of Medical Science0 个研究点目标入组 24 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
24

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
35 years 至 65 years(—)
性别
Female

入选标准

  • women ASA I,II candidate for total abdominal hysterectomy.
  • Exclusion criteria: Ages less than 35 and more than 65 years old; history of cardiac disease; hypertension; diabetes; renal or hepatic disease; no history of allergy to egg or propofol in previous anesthesia(if she had); heart rate and blood pressure changes more than 30% of baseline; any vasoactive or vasodilator injection requirement more than expected in protocol.

排除标准

  • 未提供

研究者

发起方
Tehran University of Medical Science

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