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临床试验/IRCT20210302050553N1
IRCT20210302050553N1招募中3 期

Comparison of Ropivacaine combination with Dexamethasone analgesic effect and Ropivacaine combination with dexmedetomidine on pain after cesarean section by TAP Block method

Zanjan University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
100

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 no limit(—)
性别
All

入选标准

  • ASA(American Society of Anesthesiologists) grade 1 or 2
  • The patient's ability to report the extent of their pain by criteria VAS(visual analog scale)
  • Conscious consent of the patient to participate in the study
  • Candidate for cesarean section under anesthesia with TAP(transverse abdominis plane) block

排除标准

  • History of anaphylaxis to dexmedetomidine or ropivacaine
  • History of drug abuse
  • History of coagulopathy

研究者

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