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Alopecia Areata Registry

This study is currently 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

Alopecia areata is the loss of hair in oval patches that can proceed to loss of all hair (alopecia totalis or universalis). The purpose of the registry is to collect patient information and blood samples from people with alopecia areata.

Condition
Alopecia Areata
Alopecia Totalis
Alopecia Universalis
Autoimmune Hair Loss
Alopecia Partialis

MedlinePlus related topics:  Hair Diseases and Hair Loss

Study Type: Observational
Study Design: Natural History, Cross-Sectional, Defined Population, Retrospective/Prospective Study

Further Study Details: 

Expected Total Enrollment:  2500

Study start: November 2001

Alopecia areata is a fairly common disease in which hair is lost either from part of the scalp, all of the scalp, or the entire body. It is thought to be an autoimmune disease and in some cases the disease is hereditary. The Alopecia Areata Registry will collect information and blood samples from clinically well-characterized patients with these three forms of alopecia areata: alopecia partialis (patchy loss of the scalp hair), alopecia totalis (total loss of all scalp hair), and alopecia universalis (complete loss of all hair everywhere on the body). This will be a collection of patients both in multi-generational families and in sib pairs with controls. Information from these patients will be used to search the human genome for disease-associated loci and/or genes. Researchers interested in doing pathophysiology or treatment studies of this disease will also be able to contact patients having the appropriate form of the disease for the studies in question.

Patients who have been diagnosed with alopecia areata by a dermatologist will be eligible for the registry. Patients will fill out an information form online (alopeciaareataregistry.org). Patients who have a family history or specific types of alopecia will be invited to participate in a more detailed questionnaire and physical exam and have blood samples drawn.

Eligibility

Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria


Location and Contact Information

Alopecia Areata Registry Patient Recruitment      713-792-5999 

California
      University of California, San Francisco, 1701 Divisadero Street, P.O. Box 0316, San Francisco,  California,  94143,  United States; Recruiting
Jennifer Chwalek, MD  415-476-3636    hair@derm.ucsf.edu 
Vera Price, MD,  Sub-Investigator

Colorado
      UCHSC at Fitzsimons, Departmental Mail Stop #8110, P.O. Box 6511, Aurora,  Colorado,  80045,  United States; Recruiting
Pat Somerset  720-724-4030    pat.somerset@uchsc.edu 
David Norris, MD,  Principal Investigator

Minnesota
      University of Minnesota, Minneapolis, 420 Delaware Street, MMC 98, Minneapolis,  Minnesota,  55455,  United States; Recruiting
David M. Lee  612-625-8625    aaregmn@umn.edu 
Maria Hordinsky, MD,  Sub-Investigator

New York
      Columbia University, 630 West 168th Street, VC15, New York,  New York,  10032,  United States; Recruiting
Carol Coppola, RN  212-305-6953    cc2241@columbia.edu 
Angela Christiano, PhD,  Sub-Investigator

Texas
      MD Anderson Cancer Center, Houston, 1515 Holcombe Blvd., Houston,  Texas,  77030,  United States; Recruiting
Kathleen A. Hunzicker, MD  713-794-1442    khunzick@mdanderson.org 
Madeleine Duvic, MD,  Principal Investigator

Study chairs or principal investigators

Madeleine Duvic, MD,  Principal Investigator,  M.D. Anderson Cancer Center   

More Information

Web site for the Alopecia Areata Registry

Publications

Duvic M, Norris D, Christiano A, Hordinsky M, Price V. Alopecia areata registry: an overview. J Investig Dermatol Symp Proc. 2003 Oct; 8(2): 219-21.

Study ID Numbers:  NIAMS-097
Record last reviewed:  September 2004
Record first received:  September 29, 2003
ClinicalTrials.gov Identifier:  NCT00069589
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2004-11-08
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