CTRI/2025/09/094276尚未招募2 期
To evaluate efficacy of intrauterine and sublingual and per rectal misoprostol during cesarean section in controlling postpartum haemorrhage.
Adesh university1 个研究点 分布在 1 个国家目标入组 147 人开始时间: 2025年9月16日最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 147
- 试验地点
- 1
- 主要终点
- Intraoperative and postoperative blood loss
研究概览
简要总结
In all c sections after placenta out misoprostol 600mcg will be kept by different routes like intrauterine sublingual and per rectal and the amount of blood loss will be measured and after the delivery patient will be kept under observation for any blood loss till 48hrs.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 10.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- Female
入选标准
- •All pregnant women undergoing caesarean section.
排除标准
- •Women with pre-existing coagulopathies, uterine anomalies, or known hypersensitivity to prostaglandins.
- •Patients with known as asthma, cardiac disease, acute angle closure glaucoma .Traumatic postpartum hemorrhage during caesarean section.Scar rupture Angle extension.Uterine artery cut.Scar dehiscence.
结局指标
主要结局
Intraoperative and postoperative blood loss
时间窗: During c section after placenta out and for next 48hrs post delivery
次要结局
- Need for blood transfusion(Upto 48hrs post operative)
研究者
DrHarvir Kaur
Adesh university
研究点 (1)
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