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Active, not recruiting Observational

Twin Pregnancy Cohort

NCT05144321 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2021-11-01
Last updated
2026-06-22

Condition(s) studied

Pregnant With ComplicationTwin Pregnancy With Antenatal Problem

Investigational drug(s) / intervention(s)

Impact of environment upon obstetricalneonatal and maternal adverse outcome

Impact of environment upon obstetrical: Impact of environment upon obstetrical

neonatal and maternal adverse outcome: neonatal and maternal adverse outcome

Study summary

The investigators know that multiple factors are involved in the risk of obstetric complications. The twin pregnancy model appears to be an interesting model for a bio-statistical analysis of data collected in the context of a complete pregnancy, in particular because it can reveal differences for a common exposure.

The aim of the study is to constitute a prospective cohort of twin pregnancies. The collection of data on the health of mothers, pregnancies, childbirth, and the health of twins at birth should make it possible to reveal results with sufficient statistical power for a prospective study.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion criteria: * Pregnant women * Delivery of a twin pregnancy * Gestational age \>25 weeks * Age \>18 years Exclusion criteria: * Singleton pregnancy * Miscarriage

Primary outcome measure(s)

  • maternal adverse outcome — day 1
    Pomaternal adverse outcome

Trial sites (1)

FacilityCityRegionStatus
Uhmontpellier Montpellier Montpellier
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05144321 on ClinicalTrials.gov ↗ ← All trials in France