Epidermolysis Bullosa Dystrophica Clinical Trial
Official title:
Characteristics of Patients With Recessive Dystrophic Epidermolysis Bullosa
Recessive dystrophic epidermolysis bullosa (RDEB) is a disease caused by genetic mutations in the gene for type VII collagen. Patients with RDEB develop large, severely painful blisters and open wounds from minor trauma to their skin. We are screening subjects with RDEB to evaluate characteristics of the subjects and their cells in order to develop new strategies of therapy and determine whether subjects could be candidates for treatment studies.
Status | Recruiting |
Enrollment | 70 |
Est. completion date | December 31, 2025 |
Est. primary completion date | December 31, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - Clinical diagnosis of RDEB by local dermatologist - 7 years of age or older Exclusion Criteria: -Medical instability limiting ability to travel to Stanford University Medical Center |
Country | Name | City | State |
---|---|---|---|
United States | Stanford University School of Medicine | Stanford | California |
Lead Sponsor | Collaborator |
---|---|
Stanford University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Identification of subjects with Recessive Dystrophic Epidermolysis Bullosa | Identification of subjects with Recessive Dystrophic Epidermolysis Bullosa for future studies | 4 years |
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