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Prediction of Preeclampsia by Comprehensive Markers.

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status

Completed

Conditions

Pre-Eclampsia

Study type

Observational

Funder types

Other

Identifiers

NCT03665623
preeclampsia prediction study

Details and patient eligibility

About

Preeclampsia is one of the most serious complications in pregnancy that causes maternal death and preterm delivery. Series studies has show that the competing risk model developed by the Fetal Maternal FouNdation in early pregnancy has the potential to predict preeclampsia effectively but has show crowd difference. We aim to evaluate the performance of various screening model based on FMF model in Chinese population.

Full description

The prospective multi-center observational study aimed to recruit at least 10,000 pregnant woman during the first trimester conducted among 12 medical centers in China. The medical history of each candidate was recorded , blood pressure was measured , blood sample was taken between 11 gestational weeks and 13+6 gestational weeks, to get the PlGF and PAPPA tested. Routine ultrasound was taken with measurement of the uterine artery pulsatility index. The results of the recruited patients were not released to the patients or the doctor. Pregnancy outcome was recorded as to whether the women develop preeclampsia , the SGA babies, or low birth Apgar score and other preeclampsia related adverse maternal and neonatal outcomes. The basic medical information, the mean artery pressure, the PlGF and PAPPA MOM, the UtA PI were used in combination to do the risk stratification, and to develop prediction model for Chinese people.

Enrollment

11,741 patients

Sex

Female

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. gestational weeks between 11~13+6
  2. agreed to participate the study
  3. live fetus at recruitment.

Exclusion criteria

  1. first obstetric visit beyond 14 gestational weeks
  2. artificial abortion or spontaneous abortion before 20 weeks or lost to follow-up.
  3. refused to participate the study.
  4. fetus with major chromosome or structural abnormality

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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