PACTR201802003154375已完成未知
A randomized clinical trial of sublingual versus rectal misoprostol for the prevention of postpartum hemorrhage in low resource settings
Faculty of Medicine0 个研究点目标入组 600 人开始时间: 2018年2月27日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 600
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 Year(s) 至 36 Year(s)（—）
- 性别
- Female
入选标准
- •Pregnant women at term in active labour admitted to delivery room, with singleton pregnancy, vertex presentations with no risk factors for postpartum hemorrhage.
排除标准
- •Grand multipara, operative vaginal delivery, previous uterine scar, contraindication to misoprostol or any risk factor for postpartum hemorrhage as multiple pregnancy, polyhydramnios and fetal macrosomia.
研究者
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