Alopecia Areata Registry and Immunogenetic Mechanisms
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Purpose
The goals of this study are to understand the genetic control of autoimmunity in alopecia areata (AA), to better understand the complex biology of the cycling hair follicle, and to use this knowledge to devise safe and effective treatments for this common disease.
| Condition | Intervention |
|---|---|
|
Alopecia Areata |
Behavioral: questionnaires |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Retrospective |
| Official Title: | Alopecia Areata Registry and Immunogenetic Mechanisms |
Serum, WBC.
| Estimated Enrollment: | 2000 |
| Study Start Date: | September 2001 |
| Estimated Study Completion Date: | December 2014 |
| Estimated Primary Completion Date: | December 2013 (Final data collection date for primary outcome measure) |
-
Behavioral: questionnaires
The purpose of this registry is to collect patient epidemiology data as well as to provide samples that can be used for understanding the pathogenesis of AA, especially related to its genetic basis as a complex trait. There are three ways one can assess which genes are important: association studies in unrelated individuals, identify by descent in sib-pairs, and linkage or transmission by descent in multiplex families.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Patients with alopecia areata. Controls without alopecia areata.
Inclusion Criteria:
- All patients with AA, children and adults, who have been diagnosed by a dermatologist, who is an expert in the field of alopecia. Subtypes that are allowable are alopecia universalis, alopecia totalis, patchy persistent alopecia or transient mild alopecia.
- Family members, related by blood, of these patients (preferably sib-pairs plus parents and multiplex families).
- Age matched controls from spouses or clinic patients
Exclusion Criteria:
- A person under the age of 18 years not accompanied by parent or guardian.
- A person who is unable to comprehend the informed consent and sign the consent form.
Contacts and Locations| Contact: Maria Hordinsky, MD | 612-625-1493 | hordi001@umn.edu |
| United States, Minnesota | |
| University of Minnesota | Recruiting |
| Minneapolis, Minnesota, United States, 55455 | |
| Contact: Maria Hordinsky, MD 612-625-1493 hordi001@umn.edu | |
| Principal Investigator: Maria Hordinsky, MD | |
| Principal Investigator: | Maria Hordinsky, MD | University of Minnesota - Clinical and Translational Science Institute |
More Information
No publications provided
| Responsible Party: | University of Minnesota - Clinical and Translational Science Institute |
| ClinicalTrials.gov Identifier: | NCT00177073 History of Changes |
| Other Study ID Numbers: | 0107M05422, NIH N01-AR-2249-05 |
| Study First Received: | September 13, 2005 |
| Last Updated: | February 20, 2013 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Alopecia Alopecia Areata Hypotrichosis |
Hair Diseases Skin Diseases Pathological Conditions, Anatomical |
ClinicalTrials.gov processed this record on May 16, 2013