ANgiogenic Function at NOrmal TErm on Placenta
Launched by CENTRE HOSPITALIER INTERCOMMUNAL CRETEIL · Jun 7, 2019
Trial Information
Current as of August 22, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how certain cells in the placenta, called trophoblasts, function during normal pregnancies that have reached full term (after 37 weeks). The main goal is to understand how these cells support the growth of blood vessels in the placenta, which is important for the health of both the mother and the baby. This research will involve both living participants and samples taken from the placentas after cesarean sections.
To be eligible for this study, participants should be women who are having a scheduled cesarean delivery at 37 weeks or more of pregnancy. This includes those with normal pregnancies as well as those with certain complications like gestational diabetes or pregnancy cholestasis. However, women who are under 18, have multiple pregnancies, or have specific health issues like pre-eclampsia or major fetal malformations cannot join. If you participate, you can expect to provide placenta samples after your delivery, which will help researchers learn more about how the placenta functions in different pregnancy situations.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- * Pregnancies with scheduled cesarean delivery \>37 weeks of amenorrhea:
- • strictly normal pregnancies
- • complicated pregnancies of gestational diabetes, insulin-treated or not
- • complicated pregnancies due to pregnancy cholestasis
- • spontaneous or in vitro fecondation (IVF) / Intracytoplasmic sperm injection (ICSI) pregnancies with or without oocyte donation
- Exclusion Criteria:
- • Patient's opposition
- • Age \< 18 years old
- • Women under the protection of justice
- • Multiple pregnancy
- • Known major fetal malformation
- • Pre-eclampsia and intrauterine growth retardation
- • Placental insertionnomaly
- • Type 1 diabetes
- • HIV-positive patient with HIV/hepatisis C virus (HCV) regardless of viral load
- • Patient in labour at the time of Caesarean section
- • Patient whose medical history results in medication being taken in pregnancy courses that may interfere with the biology of the trophoblast (immunomodulators in case of autoimmune diseases, anti-rejection drugs in case of transplant patients)
About Centre Hospitalier Intercommunal Creteil
Centre Hospitalier Intercommunal Créteil (CHIC) is a leading healthcare institution in the Val-de-Marne department of France, dedicated to delivering high-quality medical care and advancing clinical research. As a prominent clinical trial sponsor, CHIC collaborates with healthcare professionals and academic institutions to facilitate innovative research initiatives aimed at improving patient outcomes. The center is committed to adhering to rigorous ethical standards and regulatory guidelines, ensuring the safety and efficacy of interventions tested within its clinical trials. CHIC’s multidisciplinary approach fosters an environment of collaboration and excellence, positioning it as a key player in the advancement of medical knowledge and therapeutic options.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Creteil, , France
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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