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NCT07537751Completed

Crisaborole vs Fluticasone Propionate in Mild to Moderate Atopic Dermatitis

Comparative Study Between Topical Crisaborole 2% and Topical Fluticasone Propionate 0.05% in Treatment of Patients With Mild to Moderate Atopic Dermatitis

Source: ClinicalTrials.gov · Last updated 17 Apr 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
40 (actual)
First submitted
12 Apr 2026
Start date
1 Feb 2024
Primary completion date
1 Dec 2024
Lead sponsor
Noura Abdelmoneim Mohammed Elseessy
NCT number
NCT07537751

What you commit to

  • Study type: Interventional
  • Participants enrolled: 40
  • From 1 Feb 2024 to the primary completion date, 1 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of systemic corticosteroids, nonsteroidal systemic immunosuppressants (e.g., cyclosporine, methotrexate), or phototherapy within 4 weeks before baseline.
  • Use of topical corticosteroids, transdermal corticosteroids, topical antibiotics, or any medicated topical agent within 1 week before baseline.

Other illness

  • Significant medical condition requiring systemic medication (e.g., cancer).
  • Current clinical diagnosis of bacterial skin infection (such as abscess or impetigo).

Other

  • Severe atopic dermatitis (objective SCORAD \> 40).

Who the study is looking for

  • Children of either sex aged 1 to 12 years.
  • Clinical diagnosis of atopic dermatitis based on Hanifin and Rajka criteria.
  • Mild to moderate disease with objective SCORAD up to 40.
  • Investigator's Static Global Assessment (ISGA) score of 2 (mild) or 3 (moderate) at baseline.

Age in the registry: 1 year to 12 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Faculty of Medicine, Kafr Elsheikh University
Coordinator of this site? Confirm its status
Kafr ash ShaykhEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.