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临床试验/NL-OMON30364
NL-OMON30364已完成3 期

Misoprostol in the management of retained placenta, a safe alternative for manual removal? A randomised controlled trial - nvt

Academisch Medisch Centrum0 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
3 期
状态
已完成
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
18 至 99(—)

入选标准

  • All women with at least 25 completed pregnancy weeks and retained placenta (the placenta has not been born within 60 minutes after the birth of the child), in the abcense of postpartum haemorrhage.

排除标准

  • Excessive blood loss (>1000 ml) within 60 minutes after the delivery of the newborn. Allergy for misoprostol or one of its components.

研究者

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