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临床试验/IRCT2016040516110N3
IRCT2016040516110N3已完成未知

Clinical trial of the effect of amniotic membrane on post cesarean pain

Vice Chancellor for research of Gerash University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
90

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
no limit 至 no limit(—)
性别
Female

入选标准

  • gestational age between 38 and 42 weeks, willingness to participate in the study, experiencing the first cesarean section, live and singleton pregnancy, not having any kind of previous surgery, not smoking or consuming alcohol and drugs, no history of known diseases (such as liver and kidney dysfunction, cardiovascular, respiratory, and neuromuscular diseases, diabetes, and hypertension), and undergoing general anesthesia.
  • exclusion criteria: the surgery last for more than 90 minutes, the patients do not cooperate in measuring and recording the pain level

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research of Gerash University of Medical Sciences

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