CTRI/2020/12/029540尚未招募2 期
The efficacy and safety of intrauterine Misoprostol during Cesarean section in prevention of Primary Postpartum Hemorrhage-A Randomized Controlled Trial
Dr Nasreen Noor0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
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
入选标准
- •Gestational age of 37-40 completed weeks
- •Singleton pregnancy
- •Uncomplicated pregnancy
- •No contraindications to prostaglandins
- •No history of coagulopathy
- •Accepting to participate in the study
排除标准
- •Women with anemia(haemoglobin <8g)
- •Preterm pregnancy
- •Postterm pregnancy
- •Antepartum haemorrhage
- •History of Coagulopathy/preexisting maternal hemorrhagic disease
研究者
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