Trials / Completed
CompletedNCT00904163
Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 13 (actual)
- Sponsor
- Stanford University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Recessive dystrophic epidermolysis bullosa (RDEB) is a severe inherited blistering disease caused by the absence of type VII collagen. Patients with RDEB develop large, severely painful blisters and open wounds from minor trauma to their skin. We are screening RDEB subjects to determine additional characteristics of patients who survive to adulthood.
Conditions
Timeline
- Start date
- 2009-04-01
- Primary completion
- 2014-05-01
- Completion
- 2014-05-01
- First posted
- 2009-05-19
- Last updated
- 2014-05-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00904163. Inclusion in this directory is not an endorsement.