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临床试验/IRCT201008212854N5
IRCT201008212854N5已完成未知

Comparison of the effect of rectal Misoprostol and Syntometrin in prevention of post partum hemorrhage

Vice chancellor for Basic Sciences, Kashan University of Medical Sciences0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
200

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

年龄范围
15 years 至 50 years(—)
性别
Female

入选标准

  • pregnant women with single pregnancy and candidate for vaginal delivery Exclusion criteria: Presence of preeclampsia, hypotension, heart disease, asthma, hypertonic uterus, uterine rupture, or vaginal and cervical laceration, being high risk for postpartum bleeding such as: multiparity, uterine myoma, history of postpartum bleeding, or need for uterine curettag

排除标准

  • 未提供

研究者

发起方
Vice chancellor for Basic Sciences, Kashan University of Medical Sciences

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