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临床试验/IRCT2017031923559N9
IRCT2017031923559N9Other2 期

Compare the Ketofol and Sodium thiopental in General anesthesia patients undergoing dilatation and curettage in Alavi hospital from 2016

Vice chancellor for research, Ardabil University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
Other
发起方
入组人数
80

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
18 years 至 45 years(—)
性别
Female

入选标准

  • Vaginal bleeding; patients suspected to have an abortion; Patients candidate of uterine curettage; consent to participate in the study.
  • Exclusion criteria: contraindication to uterine curettage; sensitivity to Ketofol and Sodium thiopental

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research, Ardabil University of Medical Sciences

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