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Clinical Trials/NL-OMON48757
NL-OMON48757
Completed
Not Applicable

Prediction of preeclampsia and adverse events - PREPARE

eids Universitair Medisch Centrum0 sites400 target enrollmentTBD
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Conditionspreeclampsiatoxemia10026908

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
preeclampsia
Sponsor
eids Universitair Medisch Centrum
Enrollment
400
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\) Age \* 16 years;2\) Gestational age of at least 20 weeks and 0 days;3\) Signed written informed consent;4\) Suspected preeclampsia as a protocol defined definition , based on one or more of the following criteria:
  • •\- New onset of elevated blood pressure (BP)
  • •\- Aggravation of preexisting hypertension
  • •\- New onset of protein in urine
  • •\- Aggravation of preexisting proteinuria
  • •\- One or more other reason(s) for clinical suspicion of PE:
  • •\* PE\-related symptoms: epigastric pain, excessive edema, severe swelling (face, hands, feet), headache, visual disturbances, sudden weight gain (\>1 kg/week)
  • •\* PE\-related findings: low platelets, elevated liver transaminases, IUGR (Intra\-uterine growth restriction);OR;5\) Confirmed preeclampsia as defined by the International Society for the Study of Hypertension in Pregnancy (ISSHP)

Exclusion Criteria

  • •1\) Insufficient understanding of Dutch language

Outcomes

Primary Outcomes

Not specified

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