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Clinical Trials/NCT01804751
NCT01804751
Unknown
N/A

Prediction of Adverse Perinatal Outcome for Preeclampsia in Sichuan Province of China

West China Second University Hospital0 sitesJanuary 2016
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ConditionsPreeclampsia

Overview

Phase
N/A
Intervention
Not specified
Conditions
Preeclampsia
Sponsor
West China Second University Hospital
Primary Endpoint
maternal mortality
Last Updated
10 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

The purpose of this study is to build a model for the prediction of adverse perinatal outcome for preeclampsia in china

Registry
clinicaltrials.gov
Start Date
January 2016
End Date
December 2016
Last Updated
10 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
West China Second University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Xinghui Liu

professor

West China Second University Hospital

Eligibility Criteria

Inclusion Criteria

  • •admitted with preeclampsia or had developed preeclampsia after admission

Exclusion Criteria

  • •admitted in spontaneous labour or had achieved any component of the maternal outcome before either fulfilling eligibility criteria or collection of predictor data

Outcomes

Primary Outcomes

maternal mortality

Time Frame: within 48h of eligibility

Secondary Outcomes

  • serious cardiorespiratory morbidity(within 48h of eligibility)
  • serious central nervous system morbidity(within 48h of eligibility)
  • serious haematological morbidity(within 48h of eligibility)
  • serious hepatic morbidity.(within 48h of eligibility)
  • serious renal morbidity(within 48h of eligibility)

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