Actively Recruiting

Age: 18Years +
FEMALE
Healthy Volunteers
NCT03981653

ANgiogenic Function at NOrmal TErm on Placenta

Led by Centre Hospitalier Intercommunal Creteil · Updated on 2022-12-21

750

Participants Needed

1

Research Sites

519 weeks

Total Duration

On this page

Sponsors

C

Centre Hospitalier Intercommunal Creteil

Lead Sponsor

I

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

Collaborating Sponsor

AI-Summary

What this Trial Is About

In vivo and ex vivo study of trophoblastic angiogenic trophoblastic function in placentas from normal pregnancies, at term

CONDITIONS

Official Title

ANgiogenic Function at NOrmal TErm on Placenta

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnancies with scheduled cesarean delivery beyond 37 weeks of amenorrhea
  • Strictly normal pregnancies
  • Pregnancies complicated by gestational diabetes, treated or untreated
  • Pregnancies complicated by pregnancy cholestasis
  • Spontaneous or in vitro fertilization (IVF) / intracytoplasmic sperm injection (ICSI) pregnancies, with or without oocyte donation
Not Eligible

You will not qualify if you...

  • Patient's opposition to participate
  • Age less than 18 years old
  • Women under the protection of justice
  • Multiple pregnancy
  • Known major fetal malformation
  • Pre-eclampsia and intrauterine growth retardation
  • Placental insertion anomaly
  • Type 1 diabetes
  • HIV-positive patients with HIV or hepatitis C virus regardless of viral load
  • Patient in labor at the time of cesarean section
  • Patients taking medications during pregnancy that may affect trophoblast biology, such as immunomodulators for autoimmune diseases or anti-rejection drugs for transplant patients

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Intercommunal de Créteil

Créteil, France, 94000

Actively Recruiting

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Research Team

C

camille JUNG, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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