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临床试验/NL-OMON48687
NL-OMON48687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* - The PreRisk study

Erasmus MC, Universitair Medisch Centrum Rotterdam0 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
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

年龄范围
18 至 99(—)

入选标准

  • Women (>=18 years) with (suspected) PE with a singleton pregnancy and a
  • gestational age of >= 20 weeks and <37 weeks.
  • PE defined as de novo onset hypertension (systolic blood pressure of >=140 and
  • diastolic blood pressure of >=90mm Hg) and proteinuria (protein-to-creatinine
  • ratio >=30mg/mmol or >= 300mg/24h, or 2+ dipstick) at or after 20 weeks of

排除标准

  • Multiple pregnancies
  • Not willing to give written informed consent.
  • Other reasons than (suspected) PE requiring hospitalization
  • The presence of HELLP syndrome at time of inclusion
  • Fetal death at time of inclusion.
  • Pregnancy with a fetus affected by major congenital birth defects and/or
  • chromosomal abnormalities

研究者

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