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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Characteristics of Patients With Recessive Dystrophic Epidermolysis BullosaCollagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin Abnormalities, Skin and Connective Tissue Diseases, connective tissue disorder, epidermolysis bullosa, epidermolysis bullosa dystrophica, hereditary disease, hereditary skin disorder, skin disorder, vesiculobullous skin diseaseRecruitingNot stated2026-04-24NCT01019148

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OrganizationsLinked trials
Stanford University620

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Research sitesCityCountryLinked trials
Stanford University School of MedicineStanfordUnited States46