Actively Recruiting
Study of CCR Receptor Overexpression in Fetal Microchimeric Cells Proof of Concept Before a Potential Clinical Trial
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-09-12
160
Participants Needed
1
Research Sites
30 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
Researchers are studying the presence and behavior of foetal cells in post-partum women, focusing on their role in wound healing. The study aims to describe the gene expression profiles of these foetal cells, particularly looking at which chemokine receptors are more active in women who have wounds compared to healthy post-partum women. This approach supports the concept of using natural foetal stem cells for healing, which may avoid some risks linked to other stem cell therapies. Participants include post-partum women with venous, diabetic, sickle cell, or mixed skin ulcers, as well as age-matched post-partum women without wounds serving as controls. The study involves collecting blood and saliva samples to isolate foetal cells and perform detailed RNA sequencing to analyze their gene activity. Clinical examinations and interviews are also conducted during study visits to gather additional information. Throughout the study, researchers will analyze the isolated foetal cells using advanced sequencing techniques to understand their transcriptomic profiles. The main outcome is the single-cell transcriptomic analysis conducted over the first five months. Participants will be monitored through clinical exams and interviews, and their samples processed to identify key chemokine receptors that could guide future treatments. The study participation may last several months, with follow-up assessments as needed.
CONDITIONS
Brief Title
Fetal Cell Receptors Repertoire
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult women
- Post-partum: having been pregnant for any length of time
- Having signed a free and informed consent form
- Primiparous or multiparous
- Affiliated to a health insurance
- Patients with a venous, diabetic, sickle cell, or mixed ulcer
- Volunteers age-matched without skin ulcers (control group)
You will not qualify if you...
- Minors (for patients)
- Under court protection, curatorship, or guardianship (for patients)
- Immunocompromised patients for any reason
- Refusal of consent
- Refusal of blood and/or saliva samples for themselves or a family member
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - From Month 1 up to Month 5
Participants provide saliva and blood samples for genotyping and cell sorting to study fetal microchimeric cells.
1 to 3 visits depending on participant group
Duration - From Month 1 up to Month 5
Participants undergo clinical examinations and interviews to gather additional health information.
1 to 2 visits
Trial Site Locations
Total: 1 location
1
Dermatology unit - Cochin Hospital - APHP
Paris, Île-de-France Region, France, 75014
Actively Recruiting
Research Team
S
Sélim ARACTINGI, MD, PHD
M
Marie Benhammani-Godard
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
3
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here