跳至主要内容
临床试验/CTRI/2020/10/028736
CTRI/2020/10/028736尚未招募3 期

Comparison between preoperative versus postoperative rectal misoprostol in controlling blood loss after cesarean section- a double blind randomized controlled trial.

IPGMER0 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

  • Pregnant women at term who are electively prepared for caesarean section under regional anaesthesia.

排除标准

  • Antepartum haemorrhage, maternal hypertension, coagulation disorder, previous 2 or more caesarean section, multiple gestation, fetal macrosomia, polyhydramnios, previous uterine rupture, hypersensitivity to prostaglandin.

研究者

发起方
IPGMER

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