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Clinical Trials/ISRCTN87470468
ISRCTN87470468
Completed
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 sites370 target enrollmentNovember 20, 2015
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ConditionsTopic: Reproductive Health & ChildbirthSubtopic: Reproductive Health & ChildbirthDisease: Reproductive Health & ChildbirthPregnancy and ChildbirthPreeclampsia

Overview

Phase
未知
Intervention
Not specified
Conditions
Topic: Reproductive Health & Childbirth
Sponsor
Oxford University Hospitals NHS Trust
Enrollment
370
Status
Completed
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

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)

Registry
who.int
Start Date
November 20, 2015
End Date
July 8, 2016
Last Updated
3 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • •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

Exclusion Criteria

  • •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

Outcomes

Primary Outcomes

Not specified

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