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临床试验/NL-OMON23179
NL-OMON23179招募中不适用

Temporise or Terminate pregnancy in women with severe preeclampsia at 28-34 weeks.

Dutch consortium for studies in women's health and reproductivity.0 个研究点目标入组 1,130 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,130

研究概览

简要总结

/A

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Informed consent;
  • 2. Working knowledge of Dutch language;

排除标准

  • 1. Fetal indication for immediate delivery, ie. signs of fetal distress: Spontaneous repeated persistent unprovoked decelerations on CTG;
  • 2. Fetal death or major fetal congenital anomalies or estimated fetal weight below 500 grams;

研究者

发起方
Dutch consortium for studies in women's health and reproductivity.

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