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临床试验/CTRI/2025/09/094276
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

发起方
Adesh university
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

DrHarvir Kaur

Adesh university

研究点 (1)

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