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

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified June 2013 by Xinghui Liu, West China Second University Hospital.
Recruitment status was:  Not yet recruiting
ClinicalTrials.gov Identifier:
First Posted: March 5, 2013
Last Update Posted: August 25, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Sichuan Academy of Medical Sciences
people's hospital of Guang'an
The first people's hospital of Neijiang
Suining Central Hospital
Sichuan Provincial Maternal and Child Health Care Hospital
Chengdu Women's and Children's Central Hospital
Luzhou Medical College
pengzhou shi fuyou baojianyuan
Nanchong Central Hospital
Information provided by (Responsible Party):
Xinghui Liu, West China Second University Hospital
The purpose of this study is to build a model for the prediction of adverse perinatal outcome for preeclampsia in china


Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective

Resource links provided by NLM:

Further study details as provided by Xinghui Liu, West China Second University Hospital:

Primary Outcome Measures:
  • maternal mortality [ Time Frame: within 48h of eligibility ]

Secondary Outcome Measures:
  • serious central nervous system morbidity [ Time Frame: within 48h of eligibility ]
  • serious cardiorespiratory morbidity [ Time Frame: within 48h of eligibility ]
  • serious hepatic morbidity. [ Time Frame: within 48h of eligibility ]
  • serious renal morbidity [ Time Frame: within 48h of eligibility ]
  • serious haematological morbidity [ Time Frame: within 48h of eligibility ]

Study Start Date: January 2016
Estimated Primary Completion Date: December 2016 (Final data collection date for primary outcome measure)

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Chinese women who fulfilled a research definition of preeclampsia, and who were admitted to participating obstetric centres

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
  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: Xinghui Liu, professor, West China Second University Hospital
ClinicalTrials.gov Identifier: NCT01804751     History of Changes
Other Study ID Numbers: hx2ck2
First Submitted: March 1, 2013
First Posted: March 5, 2013
Last Update Posted: August 25, 2015
Last Verified: June 2013

Additional relevant MeSH terms:
Hypertension, Pregnancy-Induced
Pregnancy Complications