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National Registry for Ichthyosis and Related Disorders - Article


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Congenital bilateral absence of vas deferens

Absence of vas deferens; Absent vasa; CAVD; CBAVD


Clinical Trial: National Registry for Ichthyosis and Related Disorders

This study is no longer recruiting patients.

Sponsored by: National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Information provided by: National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Purpose

The ichthyoses are a family of genetic skin diseases characterized by dry, thickened, scaling skin. Dermatologists estimate that there are at least twenty varieties of ichthyosis, with a wide range of severity and associated symptoms. This registry is designed to identify people in the United States with the ichthyoses and other related disorders and to collect information about their skin ailment and how it has affected them. The database is available for review by approved research applicants. The registry is confidential and provides researchers a way to share information about studies and trials with potential participants while maintaining participants’ privacy.

Condition
Hyperkeratosis, Epidermolytic
Ichthyosiform Erythroderma, Congenital
Ichthyosis
Ichthyosis, Lamellar
Ichthyosis, X-Linked

MedlinePlus related topics:  Birth Defects;   Genetic Disorders;   Infant and Toddler Health;   Metabolic Disorders;   Skin Diseases

Study Type: Observational
Study Design: Screening, Cross-Sectional, Defined Population, Retrospective Study

Official Title: Research Registry for Inherited Disorders of Keratinization

Further Study Details: 

The purpose of this registry is to support studies aimed at determining the cause of the ichthyoses and treating them more effectively. The registry offers blinded information about well-characterized groups of individuals with specific diagnoses for study by skin biologists, pharmacologists, and others. The registry also provides information about research projects with those that have enrolled in the registry and expressed an interest in finding out about studies.

Participants may enroll in the registry by contacting the registry officials. All participants will have a phone interview with a study research nurse. Participants will be encouraged to complete an online registration form at www.skinregistry.org prior to the phone interview. Participants will be asked about their medical history, current physical condition, and other family members with skin disorders. Participants will also indicate whether they would like to be contacted about participating in clinical research.

Eligibility

Genders Eligible for Study:  Both

Criteria

Note: Accrual into this study has been discontinued as of 03/31/04.

Inclusion Criteria:

  • Diagnosis of one of the ichthyoses, erythrokeratodermas, Darier disease, Hailey-Hailey disease, palmar-plantar keratodermas, pachyonychia congenita, extensive epidermal nevi, or related disorder

Exclusion Criteria:

  • Ichthyosis Vulgaris

Location Information


Washington
      University of Washington, Seattle,  Washington,  98195,  United States

Study chairs or principal investigators

Philip Fleckman, MD,  Principal Investigator,  University of Washington   

More Information

The National Registry for Ichthyosis and Related Disorders

FIRST - Foundation for Ichthyosis and Related Skin Types

Publications

Fleckman P. Management of the ichthyoses. Skin Therapy Lett. 2003 Sep;8(6):3-7. Review.

Mayes MD, Giannini EH, Pachman LM, Buyon JP, Fleckman P. Connective tissue disease registries. Arthritis Rheum. 1997 Sep; 40(9): 1556-9. Review. No abstract available.

Study ID Numbers:  NIAMS-101
Record last reviewed:  March 2004
Last Updated:  October 13, 2004
Record first received:  December 18, 2003
ClinicalTrials.gov Identifier:  NCT00074685
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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October 10, 2008



Page Updated: September 6, 2005
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