The Effect of Gladskin on Disease Severity and the Skin Microbiome, Including Staphylococcus Aureus, in Patients With Atopic Dermatitis

This is a multi center intervention study with a placebo controlled, double blind and randomized design. After standardization of corticosteroid treatment (triamcinolone acetonide 0.1% cream), patients will be randomized in a 1:1 fashion to either treatment with Staphefekt SA.100 for 12 weeks or treatment with a placebo for 12 weeks. Topical corticosteroid use will be evaluated 2, 6, 12 and 20 weeks after start of the intervention. Swabs of the skin, nose and throat will be collected at baseline, week 2, 12 and 20.

Inclusion criteria

• Atopic dermatitis of moderate and severe severity. Defined by EASI score of 7.1 to 50 performed by the researcher at visit 1
• Topical corticosteroid use (of any type)
• 18 years or older
• Able to read patient information and provide informed consent

Exclusion criteria

• Use of systemic antibiotics or corticosteroids in the previous 2 months
• Use of Methotrexate or oral immunosuppressive agents in the previous 3 months
• Use of topical antibiotics in the previous 7 days
• Use of light therapy in the previous 3 months
• Use of Gladskin in the previous 7 days
• Contact allergy to components of the study drug (e.g., propylene glycol and glycerol)
• Clinically infected atopic dermatitis
• Existence of another skin condition, such as folliculitis or psoriasis that could interfere with the assessment of the eczema severity