跳至主要内容
临床试验/IRCT201201128677N2
IRCT201201128677N2已完成2 期

Comparison the effects of intrathecal fentanyl, pethidine or placebo added to lidocaine and epinephrine on the duration of postoperative analgesia in spinal anesthesia for elective cesarean delivery.

Vice Chancellor for research, Guilan University of Medical Sciences0 个研究点目标入组 195 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
195

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
15 years 至 40 years(—)
性别
Female

入选标准

  • being candidate for elective cesarean delivery; ASA class 1&2 and signing informed consent.
  • Exclusion criteria: addiction; contraindications for spinal anesthesia; hypersensitivity to opioids and local anesthetics; gestational hypertension; chronic itching; multi parity; having two or more surgery together and the duration of operation longer than 1.5 hours.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research, Guilan University of Medical Sciences

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