Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa
Completed
Conditions studied: Epidermolysis Bullosa Dystrophica
In brief
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.
Key facts
- Study ID
- NCT00904163
- Run by
- Stanford University
- People needed
- 13
- Starts
- 2009-04-01
- Expected to finish
- 2014-05-01
- Last updated by the study team
- 2014-05-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Stanford University School of Medicine — Stanford, California, United States
Full record on ClinicalTrials.gov
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