Phase
Condition
Eczema (Atopic Dermatitis)
Rash
Allergy
Treatment
N/AClinical Study ID
Ages 2-17 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male or female with mild to moderate atopic dermatitis, 2-17 years of age, that agreeto participate and provide written consent (and assent if applicable)
Have an investigator Global Assessment of mild to moderate atopic dermatitis (IGArating of 2-3 in the Investigator Global Assessment)
Percentage of overall body surface area of involvement (BSA) must be > 1% and mayinclude facial and intertriginous skin.
Exclusion
Exclusion Criteria:
Use within 4 weeks of baseline of systemic anti-inflammatory medication, which mayinfluence study outcome, such as systemic corticosteroids.
Application or use within 2 weeks of baseline of topical corticosteroid medications ortopical anti-inflammatory medication, which may influence study outcome.
Presence of a concurrent medical condition, which is determined by the investigator topotentially interfere with study outcomes or patient assessments.
Introduction of any other prescription medication, topical or systemic, for atopicdermatitis while participating int he study (oral antihistamines will be allowed, solong as they are neither initiated nor discontinued during the course of this study)
Amount of disease involvement that would require >60gm of cream in a 1 week period
Subjects with known allergy or sensitivity to Aquaphor Healing Ointment, Atopiclair orEpiCeram or components therein.
Study Design
Study Description
Connect with a study center
Wake Forest Baptist Medical Center
Winston-Salem, North Carolina 27157
United StatesSite Not Available

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