ACTRN12611000638932已完成4 期
Impact of pre-operative misoprostol on blood loss during and after elective cesarean delivery.
Mervat Sheikh Elarab Elsedeek Omran0 个研究点目标入组 400 人开始时间: 2011年6月23日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 400
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- o limit 至 o limit（—）
- 性别
- Female
入选标准
- •elective cesarean, full-term pregnancy, normal blood indices, non-compromised average weight fetus.
排除标准
- •labour pains, multiple pregnancy, bleeding disorder or thrombophilia, abnormal placenta(previa or accreta by ultrasound, fetal distress, preterm fetus.
研究者
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