Prospective Twin Pregnancy Cohort at Montpellier University Hospital

ConditionsPregnancyTwin
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Montpellier

About this trial

This prospective observational cohort study aims to investigate the impact of the maternal and early-life exposome on neonatal and early childhood health outcomes in twin pregnancies followed at University Hospital of Montpellier (France). Grounded in the Developmental Origins of Health and Disease (DOHaD) framework, the study focuses on how environmental, biological, and lifestyle exposures during pregnancy and the first year of life influence fetal growth, neonatal health, and early development.

A total of 120 women with monochorionic or dichorionic twin pregnancies and their 240 children will be included. Maternal exposome assessment includes air pollution exposure, lifestyle, diet, medical history, and biological measurements. Neonatal outcomes, including abnormal birth weight, will be evaluated at birth, and children will be followed until one year of age to assess growth, health events, and developmental outcomes. Biological samples collected at different times during the study will allow the assessment of chemical exposures and epigenetic markers. This study aims to generate original French twin pregnancy data and to improve understanding of environmental determinants of early-life health.

Eligibility criteria

Qualifiers

Patient of legal age (≥ 18 years)

Patient pregnant with a twin pregnancy ≥ 25 weeks of gestation

Pregnancy initially twin, triplet, or quadruplet, progressing to a twin pregnancy after spontaneous or medical embryo reduction, or after selective termination of pregnancy

Delivery planned at Montpellier University Hospital

Disqualifiers

Pregnant woman with at least one fetus presenting with a chromosomal or genetic abnormality or a polymalformative syndrome, and for whom early postnatal death is anticipated.

Planned travel preventing the study from being completed

Failure to obtain informed and written consent from the patient for participation in the study and the collection of biological samples

Patient unable to read and/or write French

Trial design

Treatments tested in this trial

  • Biological samples from the mother
  • Biological samples from the twins

Treatment groups

360 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

University Hospital, Montpellier

Lead sponsor

Institut National de la Santé Et de la Recherche Médicale, France

Collaborator