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Clinical Trial Summary

Patients with recessive dystrophic epidermolysis bullosa (RDEB) suffer from acute and chronic post-bullous wounds along with impaired skin healing. These issues are attributed not only to mucocutaneous fragility and abnormal healing directly related to quantitative and/or qualitative constitutional abnormalities of collagen VII but also to a contingent cutaneous and systemic inflammatory component. This inflammatory aspect contributes to the perpetuation of skin lesions and delayed healing. Our primary objective is to define the systemic immunological/inflammatory signature of patients with RDEB with an aim to develop a strategy that involves using stem cells with high immunomodulatory/anti-inflammatory capacity such as allogeneic placental stem cells (WJ-MSCs and trophoblasts).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06177353
Study type Observational
Source Assistance Publique - Hôpitaux de Paris
Contact Emmannuelle Bourrat, Pr
Phone +33142499090
Email emmanuelle.bourrat@aphp.fr
Status Not yet recruiting
Phase
Start date March 1, 2024
Completion date March 1, 2025

See also
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Active, not recruiting NCT05843994 - Artificial Intelligence Patient App for RDEB SCCs
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Active, not recruiting NCT04171661 - Self-Assembled Skin Substitute for the Treatment of Epidermolysis Bullosa Early Phase 1
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Completed NCT00904163 - Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa N/A
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