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临床试验/ISRCTN87470468
ISRCTN87470468已完成未知

A prospective, randomised INterventional Study evaluating the short-term PredIction of pReeclampsia/Eclampsia in pregnant women with suspected preeclampsia

Oxford University Hospitals NHS Trust0 个研究点目标入组 370 人开始时间: 2015年11月20日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
370

研究概览

简要总结

2019 Results article in https://www.ncbi.nlm.nih.gov/pubmed/31401877 results (added 14/08/2019) 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/33207235/ (added 22/03/2021) 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/34785177/ secondary analysis (added 28/04/2022)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Female aged between 18-45 years
  • 2. Pregnant >24 weeks
  • 3. Able to consent
  • 4. Singleton pregnancy
  • 5. New onset hypertension (Stratified as below – Management) AND/OR
  • 6. New onset proteinuria AND/OR
  • 7. New onset oedema/headache/visual Disturbance AND/OR
  • 8. New onset hepatic/liver tenderness AND/OR epigastric pain AND/OR
  • 9. Any other clinical suspicion of PE

排除标准

  • 1. Unable to consent
  • 2. Age less than 18 or over 45 at the time of recruitment
  • 3. Unable to speak English well enough to understand the study information
  • 4. Unwilling to participate
  • 5. Preexisting preeclampsia
  • 6. Multiple pregnancy or higher order pregnancy
  • 7. Any significant disease or disorder which in the opinion of the investigator may either put the participants at risk or may influence the result of the study or the participant’s ability to participate in the study

研究者

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