Actively Recruiting
Using Cotyledon Perfusion to Study Drugs Transfer Across the Placenta
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-09-12
2000
Participants Needed
1
Research Sites
521 weeks
Total Duration
On this page
Sponsors
A
Assistance Publique - Hôpitaux de Paris
Lead Sponsor
U
URC-CIC Paris Descartes Necker Cochin
Collaborating Sponsor
AI-Summary
What this Trial Is About
Drug prescriptions are usual during pregnancy however women and their fetuses still remain an orphan population with regard to drugs efficacy and safety clinical studies. Most xenobiotics diffuse through the placenta and some of them can alter fetus development resulting in structural abnormalities, growth or functional deficiencies. The aim of the study is to study the drug transfer using human placenta after delivery.
CONDITIONS
Official Title
Using Cotyledon Perfusion to Study Drugs Transfer Across the Placenta
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women aged 18 years or older
- Have health insurance or social security
- Pregnancy of at least 24 weeks (24th week of amenorrhea)
- Provided informed consent to participate
You will not qualify if you...
- Pre-existing maternal conditions such as diabetes-like vascular disease, arterial hypertension, or known prothrombotic disorders including history of venous thrombosis or pulmonary embolism
- Positive maternal serology for HIV, BHV, CHV, or syphilis
- Pregnancy or fetal complications including pre-eclampsia, delayed growth in utero, gestational diabetes without insulin treatment, fetal malformations, or known genetic disorders
- Under legal tutorship or curatorship, or unable to speak French
- Did not provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CIC Port-Royal-Cochin
Paris, France, 75014
Actively Recruiting
Research Team
J
Jean-Marc TRELUYER, Pr
CONTACT
M
Marie BENHAMMANI-GODARD
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
1
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