Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
ID06031714

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

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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)
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Sample Collection

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

Clinical Assessments

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

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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

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