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New Treatment of Alopecia Areata

Efficacy of Trichloroacetic Acid in Patients of Alopecia Areata : Clinico-histopathological Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05594316
Enrollment
40
Registered
2022-10-26
Start date
2019-05-01
Completion date
2022-10-19
Last updated
2022-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alopecia Areata

Keywords

alopecia areata AA

Brief summary

Abstract: Alopecia areata is believed to be an autoimmune disease resulting from a breach in the immune privilege of the hair follicles causing non scarring hair loss. Methods: our study included 40 patients from may 2019 to july 2022 diagnosed clinically, dermatoscopically and pathologically as alopecia areata Data were enrolled from department of dermatology and venereology, Al-Hussein hospital.

Detailed description

For each patient the following will be done : 1. History taking including ( age, sex, disease duration, family history, history of drug intake, smoking and history of any associated disease ). 2. All patients will give a written, informed consent for induction. 3. Basic photographs will be taken to assess site, size (by cm), number, Extent of the patch using D5300 camera with lens (18-55). 4. Patients will be subjected to 3 session of trichloroacetic acid (TCA) 35% one month apart. 5. serial photographs and dermoscopic examination every month will be done and patient will be score. 6. Efficacy will be assessed using prognostic scoring system for density, pigmentation, and texture of growing hair. 7. histopathological examination will be done before the first session and one month after third session.

Interventions

5\. Patients will be subjected to 3 session of trichloroacetic acid 35% one month apart.

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Alopecia areata multilocularis and alopecia totalis. Age from 16-60 years old. Ophiasis pattern alopecia areata.

Exclusion criteria

* Age less than 16 and more than 60years old. Alopecia areata of the face. * Patient under treatment.

Design outcomes

Primary

MeasureTime frameDescription
Mac Donald Hull and Norris grading system4 weeks after the end of treatmentregrowth of vellus hair, regrowth of sparse pigmented terminal hair, regrowth of terminal hair with patches of alopecia and regrowth of terminal hair on scalp.
Scoring of texture of regrown hairafter each session and 4 weeks after the end of treatmentFine vellus hair, Intermediate hair,Normal coarse hair
Scoring of pigmentation of regrown hairafter each session and 4 weeks after the end of treatmentPartially pigmented, Moderately pigmented, Normally pigmented
Scoring for density of hair regrowthafter each session and 4 weeks after the end of treatmentNo hair growth, 1%-25% growth, 26%-50% growth, 51%-75% growth and 76%-100% growth
Scoring of overall response at the end of the studyafter each session and 4 weeks after the end of treatmentNo response, Minimal response, Moderate response, Good response and Excellent response
histopathological changesafter each session and 4 weeks after the end of treatmentappearance of lymphocytes around hair follicle, appearance of new blood vessels and size of thickness of hair follicles
trichoscopic parametersafter each session and 4 weeks after the end of treatmentdetermine exclamation mark hairs, black dots, yellow dots and broken hairs

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026