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Prediction of Preeclampsia and Other Pregnancy Complications Following Combined Iterative Screening (PREDICTION2)

E

Emmanuel Bujold

Status

Completed

Conditions

Preeclampsia
Intra Uterine Fetal Death
Fetal Growth Restriction
Preterm Birth

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT03067298
2017-3219

Details and patient eligibility

About

Preterm birth (PTB), preeclampsia (PE), fetal growth restriction (FGR) and intra-uterine fetal death (IUFD) constitutes the main causes of perinatal morbidity and mortality and are called "Great Obstetrical Syndromes". Algorithms to predict those outcomes have been developed by combining maternal characteristics (history, age, BMI, blood pressure), biochemical (sFlt-1, β-hCG, PlGF, AFP) and sonographic (uterine artery Doppler, 3D of placenta, cervical length, nasal bone measurement, nuchal translucency) markers. Another prospective observational study ("PREDICTION study" NCT 02189148) is also ongoing, which aims to validate those algorithms at the first trimester of pregnancy.

Recent data suggest that repeating the same measurements later in pregnancy could improve the detection rates, allowing closer monitoring of high-risk patients and potential therapeutics under investigation. The current study (PREDICTION2) is an ancillary study of PREDICTION and aims at validating the use of these markers in a combined iterative manner in the prediction of preeclampsia and other obstetrical outcomes.

Full description

The objective of this study is to validate the predictive values of biophysical (maternal blood pressure); biochemical (sFlt-1, β-hCG, PlGF, and AFP) and ultrasonographic (cervical length, Doppler, 3D evaluation of the placenta, 3D nasal bone) biomarkers at several timepoints for the prediction of adverse pregnancy outcomes including preterm birth, preeclampsia, fetal growth restriction and intra-uterine fetal death.

These biomarkers will be evaluated at 14-16 weeks, 20-24 weeks and 30-34 weeks. Those specific gestational ages have been selected because they correspond to the typical clinical/hospital visits for prenatal blood and/or ultrasound screening.

Enrollment

805 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • nulliparous pregnant women participating in Prediction study (NCT02189148)

Exclusion criteria

  • <18 years old at recruitment;
  • multiple pregnancies;
  • fetal congenital malformation;
  • positive for HIV or hepatitis C;
  • fetal demise at recruitment;
  • women planning a delivery outside the participating hospitals;
  • women not able to provide an informed consent to the study.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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