PACTR201812901591120已完成4 期
The comparison of efficiency of misoprostol used in different ways in postpartum hemorrhage.
未提供0 个研究点目标入组 400 人开始时间: 2018年11月29日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 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
入排标准
- 年龄范围
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •1. Pregnant women between the ages of 18-40
- •2. Having pregnancy between 37-42 weeks
- •3. Women on vaginal delivery
- •4. Pregnant women with BMI <35
- •5. Nulliparity
排除标准
- •1. Women with multiple pregnancy
- •2. Pregnant women with myoma
- •3. Pregnant women with polyhydramnios
- •4. Pregnant women with chorioamnionitis
- •5. Pregnant women with placental abnormalities
- •6. Pregnant women with bleeding diathesis
- •7. Pregnant women with caesarean
- •8. Pregnant women with low platelet
- •9. Women who do not want to participate
- •10. Pregnant women with allergic reactions to drug
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