IRCT201405262624N17已完成3 期
Clinical trial of comparison between the effect of paracetamol (Apotel) and meperidine ( pethidine) on the pain in the first 24 hours after cesarean section.
Vice chancellor for research ,Iran University of Medical Sciences.0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 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
- no limit 至 no limit（—）
- 性别
- Female
入选标准
- •all patients after cesarean section with normal body mass index( between 18.5 and 25).
- •Exclusion criteria: Drug abuse; history of allergy to paracetamol or mepiridine; history of hepatitis; renal failure; heart failure; respiratory disease;CNS disorders; coagulopathy; sedative use; psychiatric disorders and complication of cesarean section.
排除标准
- 未提供
研究者
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