IRCT138812223548N1已完成2 期
Comparison of misoprostrol and oxytocin in reduction of postpartum hemorrhage
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 300
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
- •pregnant women with singleton pregnancy, cephalic, spontaneous and induced delivery, term pregnancy. Exclusion criteria: instrumental delivery, TL during 24h after delivery, past history of abruption placenta, history of asthma, coagulopathy, history of postpartum hemorrhage, history of C/S.
排除标准
- 未提供
研究者
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