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临床试验/IRCT2013080514275N1
IRCT2013080514275N1已完成2 期

Comparison of sub-lingual misoprostol and intravenous oxytocin in controlling of hemorrhage after cesarean section.

Vice Chancellor for Research of Semnan University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
100

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
no limit 至 no limit(—)
性别
Female

入选标准

  • singleton pregnant women; elective cesarean delivery; Gravid 1, 2 (maximum one section)
  • Exclusion criteria: Patients with preeclampsia (high blood pressure and protein in the urine); diseases cardiovascular diseases; asthma; uterine rupture; uterine leiomyoma or a women with a history of excessive bleeding after childbirth.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for Research of Semnan University of Medical Sciences

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