CTRI/2024/01/062091尚未招募3 期
Reduction in blood loss in Caesarean delivery following use of intra-uterine and rectal Misoprostol -A Comparative Study
il0 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
- 3 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
- •Antenatal women more than 37 weeks of gestation planned for Elective LSCS
排除标准
- •Fetal Anomalies
- •Maternal Medical disorders
- •Placenta previa ,Placenta accreta spectrum
- •Known allergy to prostaglandin
- •Previous 2 LSCS or more
- •Patients requiring blood transfusion
研究者
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