drugset / Trial / NCT07537751

Crisaborole vs Fluticasone Propionate in Mild to Moderate Atopic Dermatitis

NCT07537751

Completed 40 enrolled Noura Abdelmoneim Mohammed Elseessy
RandomizedParallel-groupDouble-blindTreatment

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.

Timeline

Start
2024-02-01
Primary completion
2024-12-01
Completion
2025-03-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Crisaborole Small molecule 2 % Topical
Comparator Fluticasone propionate Other / unclassified 0.05 % Topical

Indications