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Establishment of the National Epidermolysis Bullosa Registry

N

National Center for Research Resources (NCRR)

Status

Completed

Conditions

Epidermolysis Bullosa

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT00004761
199/11706
RU-0170195

Details and patient eligibility

About

OBJECTIVES: I. Develop a large roster of well-characterized patients with various forms of inherited and acquired epidermolysis bullosa (EB).

II. Generate a large data bank of clinical, historical, and genetic information concerning these patients.

III. Accumulate donated tissue specimens, including selected cells and DNA, from selected patient subsets for the establishment of permanent tissue cell banks.

IV. Promote and facilitate research in EB.

Full description

PROTOCOL OUTLINE: Patients are enrolled by mail or clinic visit at 1 of 4 clinical centers. Clinical, epidemiological, and laboratory data are collected.

Medical and family histories are obtained in a detailed interview in person, by phone, or by mail. Diagnostic studies to confirm the type of epidermolysis bullosa are performed as indicated. A pedigree chart is completed on the first affected family member entered.

Selected patients are followed at least biannually. A study duration of approximately 10 years is anticipated.

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

  • Clinical diagnosis of epidermolysis bullosa

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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