Clinical Trial: Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa

Study Status: Completed
Recruit Status: Completed
Study Type: Observational

Official Title: Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa

Brief 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.

Detailed Summary:
Sponsor: Stanford University

Current Primary Outcome:

Original Primary Outcome:

Current Secondary Outcome:

Original Secondary Outcome:

Information By: Stanford University

Dates:
Date Received: May 15, 2009
Date Started: April 2009
Date Completion:
Last Updated: May 15, 2014
Last Verified: May 2014