Response of Topical Capsaicin in Alopecia Areata

NCT ID: NCT00176969

Last Updated: 2014-06-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

1997-08-31

Study Completion Date

2000-06-30

Brief Summary

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It has been postulated that Alopecia Areata (AA) is, at least in part, a neurologically mediated disease. Research supporting this theory includes the finding that nerves surrounding the hair follicles are collapsed. We want to take this research a step further and show that not only are these perifollicular nerves collapsed, but that their function is also impaired.

Detailed Description

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To assess the function of perifollicular scalp nerves in AA we will look at the response of these nerves to the topical medication capsaicin. Under normal circumstances topical capsaicin is known to target nerves in the peripheral nervous system causing short-term release of the neuropeptide Substance P (SP) as well as long-term transient depletion of SP. We expect the AA patients will respond abnormally to topical capsaicin treatment.

Conditions

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Alopecia Areata

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Interventions

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Capsaicin

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Must have alopecia totalis or universalis.
* Be in good health.
* Not be taking any medications including topical medications
* Be 18 years or older.
* Be willing to apply study medication or vehicle as directed, comply with instructions and commit to follow-up visits.
* Not have had hair chemically treated (including colored hair, permed hair, etc) within the month prior to the study.

Exclusion Criteria

* Absence of extensive alopecia areata.
* People not in good health.
* People taking medications.
* Allergies to capsaicin.
* Presence of irritated or visibly inflamed scalp.
* Having had hair chemically treated (including colored hair, permed hair, etc.) within the month prior to study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Minnesota

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Maria Hordinsky, MD

Role: PRINCIPAL_INVESTIGATOR

University of Minnesota

Marna Ericson, Ph D

Role: PRINCIPAL_INVESTIGATOR

University of Minnesota

Locations

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University of Minnesota

Minneapolis, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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9707M00122

Identifier Type: -

Identifier Source: org_study_id

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