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临床试验/IRCT2017012320258N28
IRCT2017012320258N28已完成未知

? Comparison effect of addition of Dexmedetomidine and Fentanyl to ?Lidocaine 5% in spinal anesthesia to increase postoperative analgesia in ?women candidate elective ?cesarean

Vice chancellor for Research, Arak University of Medical Sciences0 个研究点目标入组 84 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
84

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 35 years(—)
性别
Female

入选标准

  • 18 to 35 years; single pregnancy; candidate ?cesarean with spinal anesthesia; elective ?cesarean.
  • Exclusion criteria: multiple pregnancy; allergy for Fentanyl and dexmedetomidine; infection in site of spinal anesthesia; lack of consent.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for Research, Arak University of Medical Sciences

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