Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa

Not Recruiting

Trial ID: NCT00904163

Age - 18 Years-N/A Gender - All Accepting Healthy Volunteers - No

Purpose

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.

Official Title

Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa

Stanford Investigator(s)

M. Peter Marinkovich, MD
M. Peter Marinkovich, MD

Associate Professor of Dermatology

Paul A. Khavari, MD, PhD
Paul A. Khavari, MD, PhD

Carl J. Herzog Professor of Dermatology in the School of Medicine

Eligibility


Inclusion Criteria:1. Clinical diagnosis of RDEB by local dermatologist. 2. 18 years of age
or more and willing to give consent. Exclusion Criteria:1. Medical instability limiting
ability to travel to Stanford University Medical Center.

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Not Recruiting

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Emily Gorell, MS
650-721-7166

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