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RecruitingNCT06564805

Clinical Trial on the Efficacy of Intralesional Triamcinolone Versus Candida Albicans Antigen in Treating Alopecia Areata

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Universidad Autonoma de Nuevo Leon · Academic / Other
Sex
All
Age
6 Years
Healthy volunteers
Not accepted

Summary

The efficacy of two intralesional treatment modalities for alopecia areata will be determined. Thirty patients over the age of 6 with the diagnosis of alopecia areata on the scalp, with an extension of less than 50%, will be included. A comparison will be made between the effectiveness of intralesional Triamcinolone (standard first-line treatment) and intralesional Candida albicans antigen, with serial clinical and trichoscopic pictures at follow-up to evaluate the clinical response and associated adverse effects.

Conditions

Interventions

TypeNameDescription
DRUGCandida Albicans Antigen Injectionsubcutaneous administration of Candida albicans antigen

Timeline

Start date
2024-08-20
Primary completion
2025-07-30
Completion
2025-12-31
First posted
2024-08-21
Last updated
2024-08-21

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT06564805. Inclusion in this directory is not an endorsement.

Clinical Trial on the Efficacy of Intralesional Triamcinolone Versus Candida Albicans Antigen in Treating Alopecia Areat (NCT06564805) · Clinical Trials Directory