Treatment of Atopic Dermatitis With Different Orders of Application of Locoid Lotion and Hylatopic Plus Cream

This is an interventional treatment trial for Atopic Dermatitis focused on measuring Atopic Dermatitis, AD Read More

Inclusion Criteria:

• subjects of at least 3 months of age.
• clinical diagnosis of stable mild to moderate AD using the Hanifin and Rajka criteria for diagnosing AD
• AD lesions of similar size and severity of bilateral anatomic location
• a SPGA score of 2 or 3 and at least 10% BSA involvement at baseline
• in good health, without evidence of disease process(es) that would present patient safety concerns or confounding factors for assessment of study objectives
• able and willing to understand and sign an informed consent (or if applicable parent or legal guardian sign an informed consent),
• able and willing to agree to requirements and restrictions of the study
• Subjects who are willing to discontinue all systemic corticosteroids, immunomodulators, ultra violet light therapy or other medication (investigational or otherwise) that may have an effect on atopic dermatitis disease progression for 30 days prior to the baseline measurement.
• Subjects on a stable maintenance therapy (at least 30 days of use prior to baseline) of antihistamines and/or nasal spray containing corticosteroids for the treatment of bronchial asthma or allergic rhinitis, and antibiotics for the treatment of acne will be allowed.
• Subjects who are willing to discontinue use of topical treatments for AD including, but not limited to, corticosteroids, immunomodulators, vitamin D treatments, retinoids, topical antihistamines for at least 14 days prior to baseline
• Subjects who are willing to discontinue use of oral antibiotic therapy for at least 7 days prior to baseline, unless prescribed for acne treatment as previously described
• Subjects with no known allergy to any of the study product ingredients
• Women of childbearing potential must be willing to use a form of birth control during the study. For the purpose of this study, the following are considered acceptable methods of birth control: oral contraceptives, Norplant, Depo-Provera, double barrier methods (e.g., condom and spermicide) and abstinence.

Exclusion Criteria:

• immunocompromised patients, or subjects with extensive disease that could not reasonably be controlled with topical therapy
• history or evidence of other conditions that would interfere with the evaluation of the study medication
• subjects desiring excessive or prolonged exposure to UV light (e.g. sunlight/tanning beds) during the study
• Use of topical medications for AD or any other medical condition.
• Subjects currently involved in another clinical research study.
• Subjects, who are pregnant, breast feeding or planning a pregnancy.
• Subjects with clinically significant unstable medical or mental disorders.
• Subjects who are unwilling or unable to comply with the requirements of the protocol.