drugset / Trial / NCT06564805

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

NCT06564805

Recruiting 30 enrolled Autonomous University of Nuevo León
RandomizedParallel-groupTriple-blindTreatment

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.

Timeline

Start
2024-08-20
Primary completion
2025-07-30
Completion
2025-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Candida albicans antigen Unknown 0.1 ml Subcutaneous

Indications