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临床试验/NL-OMON22891
NL-OMON22891招募中不适用

The PreRisk calculator in suspected or confirmed preeclampsia: A new tool to safely reduce the number of unnecessary admissions’

one0 个研究点目标入组 864 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
one
入组人数
864

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

入选标准

  • Women with a singleton pregnancy
  • Age = 18 years
  • Gestational age = 20 weeks and <37 weeks
  • Suspected or confirmed PE
  • Alive fetus without fetal distress requiring immediate delivery

排除标准

  • - Other reasons than (suspected) PE requiring hospitalization.
  • - The presence of partial (HELLP) syndrome at time of inclusion.
  • - The presence of fetal death at time of inclusion.
  • - Pregnancy with a fetus affected by major congenital birth defects and/or chromosomal abnormalities
  • - Unable to provide written informed consent.

研究者

发起方
one

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