Fetal Cell Receptors Repertoire
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorAssistance Publique - Hôpitaux de Paris
About this trial
The purpose of this study is to describe the transcriptomic profile of foetal cells in post-partum and more specifically to determine which chemokine receptors are overexpressed in foetal cells in post-partum women with wounds To do so, the investigators will isolate foetal cells from the peripheral blood of healthy controls post partum women as well as from post partum women with skin ulcers and then perform RNA sequencing.
Eligibility criteria
Qualifiers
Adult women,
Post-partum: having been pregnant for any length of time,
Having signed a free and informed consent form,
Primiparous or multiparous,
Disqualifiers
Minors (for patients)
Under court protection, curatorship, guardianship (for patients)
Immunocompromised patients for any reason whatsoever
Refusal of consent
Trial design
Treatments tested in this trial
- Saliva sampling
- Blood sampling
- Interviews
- Clinical examination
Treatment groups
160 Participants
are divided into 3 treatment groupsSponsors and collaborators
Assistance Publique - Hôpitaux de Paris
Lead sponsor
URC-CIC Paris Descartes Necker Cochin
Collaborator
Source ClinicalTrials.gov