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Alopecia Areata Registry (NAAR)

This study is currently recruiting participants. (see Contacts and Locations)
Verified April 2014 by M.D. Anderson Cancer Center
Sponsor:
Collaborator:
National Alopecia Areata Foundation
Information provided by (Responsible Party):
M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier:
NCT00069589
First received: September 29, 2003
Last updated: April 25, 2014
Last verified: April 2014
  Purpose

Alopecia areata is the loss of hair in 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

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Alopecia Areata Registry and Immunogenetic Mechanisms

Resource links provided by NLM:


Further study details as provided by M.D. Anderson Cancer Center:

Primary Outcome Measures:
  • Alopecia Areata Registry [ Time Frame: Registration on-going ] [ Designated as safety issue: No ]
    Database registration of participants via collection of participant epidemiology data.


Biospecimen Retention:   Samples With DNA

DNA will be analyzed to learn the link between gene markers of traites of alopecia areata. Sera will be used to analyse cytokins. Lymphocytes will be used for the creation of B-cell lines.


Estimated Enrollment: 3100
Study Start Date: November 2001
Estimated Study Completion Date: November 2099
Estimated Primary Completion Date: November 2099 (Final data collection date for primary outcome measure)
Detailed Description:

Alopecia areata is a condition in which hair is lost either from part of the scalp, all of the scalp, or the entire body, and it affects 1% to 2% of the population. 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 in multi-generational families, twins, single patients with patchy, persistent transient alopecia areata or long-standing alopecia totalis/universalis and with controls (persons unaffected and not related to alopecia patients). 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:   Yes
Sampling Method:   Probability Sample
Study Population

Patients with alopecia areata (AA), both children and adults, who have been diagnosed by a physician with alopecia universalis, alopecia totalis, patchy persistent AA, or transient mild AA. Family members (related by blood) of these patients, preferably sib-pairs plus parents and multiplex families(persons with at least three family members with AA or alopecia universalis and alopecia totalis).

Also, healthy individuals who are unaffected, non-blood related individuals and do not live in the same household with alopecia areata patient are needed as controls.

Criteria

Inclusion Criteria

  • Diagnosed with alopecia areata by a dermatologist
  • United States resident

Accepts Health Volunteers: Non blood-related individuals who are unaffected with alopecia areata and do not live in the same household with alopecia areata patient.

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00069589

Contacts
Contact: Alopecia Areata Registry Patient Recruitment 713-792-5999 alopeciaregistry@mdanderson.org
Contact: Alopecia Areata Registry Toll Free Number 1-866-837-1050

Locations
United States, California
University of California, San Francisco Recruiting
San Francisco, California, United States, 94143
Contact: Charles Chiang, MD    415-353-4333      
Sub-Investigator: Vera Price, MD         
United States, Colorado
University of Colorado - UCHSC - Health Science Center at Fitzsimons Recruiting
Aurora, Colorado, United States, 80010-7163
Contact: Lisa Maestas    303-724-4032    Lisa.Maestas@uchsc.edu   
Sub-Investigator: David Norris, MD         
United States, Minnesota
University of Minnesota Recruiting
Minneapolis, Minnesota, United States, 55455
Contact: Chelsy Jungbluth    612-625-9338      
Sub-Investigator: Maria Hordinsky, MD         
United States, New York
Columbia University Recruiting
New York, New York, United States, 10032
Contact: Carol Coppola, RN    212-305-6953    cc2241@columbia.edu   
Sub-Investigator: Angela Christiano, PhD         
United States, Texas
M.D. Anderson Cancer Center Recruiting
Houston, Texas, United States, 77030
Contact: Joyce Osei, MPH, MHA    713-794-1442    jsosei@mdanderson.org   
Principal Investigator: Madeleine Duvic, MD         
Sponsors and Collaborators
M.D. Anderson Cancer Center
National Alopecia Areata Foundation
Investigators
Principal Investigator: Madeleine Duvic, MD M.D. Anderson Cancer Center
  More Information

Additional Information:
Publications:
Barahmani N, Yang Y, Lopez A, Duvic M. Atopic alopecia areata patients have increased serum Th1 Cytokine profiles. 66th Annual meeting of Society for Investigative Dermatology. St.Louis, MO, May 2005. JID 124 (4): A100, 2005.
Breuer-McHam J, Hunzicker K, Barahmani N, Zhang Q, Babu D, Christiano A, Hordinsky M, Norris D, Price V, Duvic, M. Epidemiologic and disease associations in participants of the national alopecia areata (NAAR) registrants. Accepted by Society for Investigational Dermatology, April 12, 2004. JID 122 (3): A107, 2004.
de Andrade M, Barahmani N, Hunzicker K, Zhang Q, Joan Breuer- McHam, Joyce Osei, Daniel Babu, Qingyi Wei, Reveille J, Duvic M. HLA Class II associations confirm alopecia areata phenotypic subsets. 66th Annual meeting of Society for Investigative Dermatology. St. Louis, MO, May 2005.JID 124 (4): A107, 2005.

Responsible Party: M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier: NCT00069589     History of Changes
Obsolete Identifiers: NCT00177073
Other Study ID Numbers: NIAMS-097, HHSN268200682279C
Study First Received: September 29, 2003
Last Updated: April 25, 2014
Health Authority: United States: Federal Government

Keywords provided by M.D. Anderson Cancer Center:
Baldness
Autoimmunity
Hair
Alopecia Areata
Alopecia Partialis
Alopecia Totalis
Alopecia Universalis
Autoimmune Hair Loss

Additional relevant MeSH terms:
Alopecia
Alopecia Areata
Hypotrichosis
Hair Diseases
Skin Diseases
Pathological Conditions, Anatomical

ClinicalTrials.gov processed this record on September 18, 2014