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Study of the Physiology of Pre-eclampsia and Vascular IUGR With Constitution of a Biological Collection

Recruiting
Conditions
Pre-Eclampsia
Interventions
Other: collect of placenta, blood and urinary samples at delivery
Registration Number
NCT03626233
Lead Sponsor
Centre Hospitalier Intercommunal Creteil
Brief Summary

Preeclampsia and intrauterine growth retardation (IUGR) are serious and frequent pathologies, specific to pregnancy. They represent 70 000 new cases a year, or 9% of pregnancies and cause 50,000 premature births per year in France. The consequences in terms of morbidity and perinatal morbidity and the medical and economic costs make it an issue public health. Pre-eclampsia associates maternal hypertension with dysfunction kidney. There is no cure for pre-eclampsia or IUGR vascular during pregnancy. These pathologies invariably evolve towards a maternal and / or fetal aggravation sometimes very fast. Primary prevention and secondary education and screening for these pathologies are still insufficient. A better understanding of the pathophysiology of these placental vascular pathologies is necessary for the development of supported medical, obstetric and pediatric that will improve the state of health maternal and neonatal

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
500
Inclusion Criteria
  • pregnant women
  • With or without vascular pathology
Exclusion Criteria
  • refusal to participate
  • multiple pregnancy
  • major fetal malformation diagnosed during pregnancy follow-up

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Vascular groupcollect of placenta, blood and urinary samples at deliveryPregnant women with vascular pathology
Control groupcollect of placenta, blood and urinary samples at delivery* Pregnancy without any vascular complication * Delivery before or after 37 weeks of gestation (GW) * In case of delivery after 37GW: birth by cesarean delivery
Primary Outcome Measures
NameTimeMethod
genomic analysis on placentaday of delivery

by chromatin immunoprecipitation-sequencing (ChIP-seq)

Secondary Outcome Measures
NameTimeMethod
genomic analysis on placentaday of delivery

by immunohistochemistry an polymerase chain-reaction

PLGF blood levelday of delivery
sFlt1 blood levelday of delivery
genomic analysis on bloodday of delivery

by ChIP-seq

VEGF blood levelday of delivery
sKDR blood levelday of delivery

Trial Locations

Locations (1)

CHi Creteil

🇫🇷

Creteil, France

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