Fetal Cell Receptors Repertoire
Recruiting
N/A
Interventional Study
Venous Ulcer
Sickle Cell Ulcer
Diabetic Ulcer
Post-partum Women
Mixed Ulcer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 160 (estimated)
- Sponsor
- Assistance Publique - Hôpitaux de Paris · Other
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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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
Common criteria :
* 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 :
\- Patients with a venous, diabetic or sickle cell ulcer,…
Contacts