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临床试验/IRCT2014040517081N1
IRCT2014040517081N1已完成未知

ower uterine compression sutures for the Treatment of Postpartum Hemorrhage due to Placenta Previa Complete centralis; prospective study

Department of Obstetrics and Gynecology, Benha University Hospital0 个研究点目标入组 25 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
25

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
22 years 至 45 years(—)
性别
Female

入选标准

  • All patients had placenta previa complete centralis (25). The inclusion criteria are a gestation age of = 28 weeks and antepartum hemorrhage; intraoperative postpartum hemorrhage and discovery of a placenta previa; successful removal of the placenta
  • exclusion criteria: shock due to massive blood loss ,failure of successful removal of the placenta

排除标准

  • 未提供

研究者

发起方
Department of Obstetrics and Gynecology, Benha University Hospital

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