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临床试验/PACTR201302000466116
PACTR201302000466116已完成未知

Open Randomized Cluster Clinical Trial of Community Distribution of Oral Misoprostol for Prevention of Post Partum Haemorrhage In Uganda

PACE0 个研究点目标入组 4,500 人开始时间: 2012年11月27日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
4,500

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

年龄范围
18 Year(s) 至 52 Year(s)(—)
性别
Female

入选标准

  • At the individual level, the study included pregnant women at 28 weeks (7months) or more of gestation determined from LNMP or clinical examination, had to be residents of Mubende or Mityana districts, above 18 years of age and anticipating uncomplicated vaginal delivery. Only women who gave informed written consent were included in the study. At the cluster level, the study included parishes projected to have at least 100 births within the study period.

排除标准

  • The study excluded pregnant women with diagnosed multiple pregnancy,
  • chronic medical conditions
  • and reported hypersensitivity to prostaglandins or inability to give informed consent (e.g. mental health illness), as assessed by the recruiting research assistant

研究者

发起方
PACE

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