Comparison of the Efficacy and Safety of Two Topical Creams for Pediatric Atopic Dermatitis
Completed · Phase 4
Conditions studied: Atopic Dermatitis
In brief
This study compares the effectiveness of two topical creams for atopic dermatitis in pediatric subjects. Subjects will be randomly assigned to use one of the two creams twice daily for 6 weeks or until clear.
Key facts
- Study ID
- NCT00828412
- Run by
- Promius Pharma, LLC
- People needed
- 100
- Starts
- 2009-03-01
- Expected to finish
- 2009-08-01
- Last updated by the study team
- 2017-01-30
Who can join
Age: 0 and older, up to 12. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- at least 3 months of age and less than 13 years of age
- atopic dermatitis of moderate severity
You may not qualify if…
- pregnant or lactating
- treatment of atopic dermatitis with topical product in the 14 days prior to Baseline
- treatment of atopic dermatitis with systemic product in the 30 days prior to Baseline
- serious or uncontrolled medical condition
- active infection
- significant use of inhaled, intranasal, or intraocular corticosteroid
Where it is running
- National Jewish Health — Denver, Colorado, United States
- Northwestern University — Chicago, Illinois, United States
- Wake Forest University Health Sciences — Winston-Salem, North Carolina, United States
- Dermatology Research Associates — Cincinnati, Ohio, United States
- University of Texas — Houston, Texas, United States
Full record on ClinicalTrials.gov
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