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临床试验/IRCT2016041125648N3
IRCT2016041125648N3已完成未知

Sublingual Misoprostol to Reduce Blood Loss in Cesarean Delivery

Vice Chancellor for Research of Mashhad University of Medical Sciences0 个研究点目标入组 90 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
90

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

  • Inclusion criteria are: any of post partum hemorrhage risk factors in term pregnancies like uterine over distention (macrosomia or multiple pregnancies); arrested descent labor; prolonged induction.
  • Exclusion criteria are: coagulopathies; anemia; adhesion bands,; organ damage during surgery (intestine; colon; Bladder; etc); allergy for prostaglandins, abnormal placenta; need for extended surgery incision and underlying diseases (diabetes mellitus; hypertension; ischemic heart disease; etc).

排除标准

  • 未提供

研究者

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

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