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Crisaborole vs Fluticasone Propionate in Mild to Moderate Atopic Dermatitis
Sponsor: Noura Abdelmoneim Mohammed Elseessy
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.
Official title: Comparative Study Between Topical Crisaborole 2% and Topical Fluticasone Propionate 0.05% in Treatment of Patients With Mild to Moderate Atopic Dermatitis
Key Details
Gender
All
Age Range
1 Year - 12 Years
Study Type
INTERVENTIONAL
Enrollment
40
Start Date
2024-02-01
Completion Date
2025-03-01
Last Updated
2026-04-17
Healthy Volunteers
No
Conditions
Interventions
Crisaborole 2% topical ointment
Crisaborole 2% topical ointment applied in a thin layer to all affected atopic dermatitis lesions twice daily for 6 weeks, followed by twice-weekly application for 12 weeks as maintenance in patients who achieve more than 75% improvement in SCORAD at Week 6.
Fluticasone propionate 0.05% topical cream
Fluticasone propionate 0.05% topical cream applied in a thin layer to all affected atopic dermatitis lesions twice daily for 6 weeks, followed by twice-weekly application for 12 weeks as maintenance in patients who achieve more than 75% improvement in SCORAD at Week 6.
Locations (1)
Faculty of Medicine, Kafr Elsheikh University
Kafr ash Shaykh, Kafr el-Sheikh Governorate, Egypt