Clinical Trial

Crisaborole vs Fluticasone Propionate in Mild to Moderate Atopic Dermatitis

Completed
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Summary
This randomized, double-blind trial compared topical crisaborole 2% with topical fluticasone propionate 0.05% in children aged 1-12 years with mild to moderate atopic dermatitis. Forty patients were assigned to receive either crisaborole or fluticasone twice daily on affected areas for 6 weeks, with responders (\>75% improvement in SCORAD) continuing the same treatment twice weekly for 12 weeks as maintenance. The study evaluated improvement in disease severity using SCORAD and ISGA, pruritus scores, disease-free survival, and local tolerability. Both treatments were effective and well tolerated; fluticasone produced faster short-term improvement, while crisaborole showed a trend toward fewer relapses and similar overall safety in this pediatric population.
Trial Details
NCT Number NCT07537751
Lead Sponsor Noura Abdelmoneim Mohammed Elseessy
Conditions Atopic Dermatitis, Eczema
Enrollment 40 participants
Start Date 2024-02-01
Primary Completion 2024-12-01 (estimated)
Study Completion 2025-03-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-17