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

NCT01804751 | Unknown

• 1 other identifier: hx2ck2
• Study Type: observational
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

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

Conditions

Preeclampsia

Outcome Measures

Primary Outcomes (1)

• maternal mortality

  within 48h of eligibility

Secondary Outcomes (5)

• serious central nervous system morbidity

  within 48h of eligibility

• serious cardiorespiratory morbidity

  within 48h of eligibility

• serious hepatic morbidity.

  within 48h of eligibility

• serious renal morbidity

  within 48h of eligibility

• serious haematological morbidity

  within 48h of eligibility

Eligibility Criteria

• Sex: female
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Chinese women who fulfilled a research definition of preeclampsia, and who were admitted to participating obstetric centres

You may qualify if:

• admitted with preeclampsia or had developed preeclampsia after admission

You may not qualify if:

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

Sponsors & Collaborators

• West China Second University Hospital: lead
• Sichuan Academy of Medical Sciences: collaborator
• Guang'an people's hospital of Sichuan province: collaborator
• The First People's Hospital of Neijiang: collaborator
• Suining Central Hospital: collaborator
• Sichuan Provincial Maternal and Child Health Care Hospital: collaborator
• Chengdu Women's and Children's Central Hospital: collaborator
• Luzhou Medical College: collaborator
• pengzhou shi fuyou baojianyuan: collaborator
• Nanchong Central Hospital: collaborator

MeSH Terms

Conditions

Pre-Eclampsia

Condition Hierarchy (Ancestors)

Hypertension, Pregnancy-Induced; Pregnancy Complications; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: professor

Study Record Dates

• First Submitted: March 1, 2013
• First Posted: March 5, 2013
• Study Start: January 1, 2016
• Primary Completion: December 1, 2016
• Last Updated: August 25, 2015

Record last verified: 2013-06