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

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

Study Overview

• Status: Unknown
• Conditions: Preeclampsia

• Study Type: Observational

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Child; Adult; Older Adult
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

• Sampling Method: Non-Probability Sample

Study Population

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

Description

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

Study Plan

How is the study designed?

Design Details

• Observational Models: Cohort
• Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
maternal mortality	within 48h of eligibility

Secondary Outcome Measures

Outcome Measure	Time Frame
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

Collaborators and Investigators

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

Study record dates

Study Major Dates

• Study Start: January 1, 2016
• Primary Completion (Anticipated): December 1, 2016

Study Registration Dates

• First Submitted: March 1, 2013
• First Submitted That Met QC Criteria: March 1, 2013
• First Posted (Estimate): March 5, 2013

Study Record Updates

• Last Update Posted (Estimate): August 25, 2015
• Last Update Submitted That Met QC Criteria: August 24, 2015
• Last Verified: June 1, 2013

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pregnancy Complications; Hypertension, Pregnancy-Induced; Pre-Eclampsia
• Other Study ID Numbers: hx2ck2