跳至主要内容
临床试验/CTRI/2010/091/006136
CTRI/2010/091/006136已完成未知

Comparative study of combined per rectal misoprostol and intravenous oxytocin infusion versus intravenous oxytocin infusion in third stage of labour.

Bankura Sammilani Medical College Hospital0 个研究点目标入组 500 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
500

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

  • Women who will have spontaneous normal delivery of a live, singleton neonate, and absence of any contraindications for misoprostol or oxytocin use.

排除标准

  • women delivered by cesarean, or had a history of antepartum hemorrhage or bleeding tendency. The diagnosis of hypertensive disorder with pregnancy or the need for anticoagulants also will serve as exclusion criteria.

研究者

发起方
Bankura Sammilani Medical College Hospital

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