The Impact of Dupilumab on Quality of Life in Moderate to Severe Atopic Dermatitis Patients

    Not Recruiting
  • participants needed
  • sponsor
    University of California, San Francisco
Updated on 10 August 2022


This is a single-arm, open-label study, which will examine the effect of dupilumab on quality of life in atopic dermatitis patients.


This is a single center, open-label study, which will examine the effect of dupilumab on quality of life in atopic dermatitis (AD). Thirty patients with moderate to severe AD will receive dupilumab for a treatment period of 52 weeks (i.e. last injection on week 48). Improvement in patient quality of life after 52 weeks of treatment with dupilumab will be evaluated using validated dermatologic and non-dermatologic psychometric instruments. The primary endpoint is the improvement in quality of life measured by change in Psychological General Well-Being scale (PGWB) at Week 16 from baseline. Additionally, patients will be given a video recording device to document their experience with the study drug at home. Video footage of patient experiences will be compiled at the end of the study. The compiled video footage will subsequently be watched and analyzed to further understand the experiences of atopic dermatitis patients, and how undergoing dupilumab treatment alters these patients' experiences and attitudes with their skin disease.

Condition Eczema, Eczema (Atopic Dermatitis - Pediatric), ATOPIC DERMATITIS, Eczema (Atopic Dermatitis), ATOPIC DERMATITIS, Dermatitis, Atopic, Dermatite Atopique, Eczéma (Dermatite Atopique), Dermatitis, Hand Dermatitis, Eczema (Atopic Dermatitis), Dermatitis, Atopic, Hand Dermatitis, Eczema (Atopic Dermatitis - Pediatric), Atopic Dermatitis Eczema, Eczéma (Dermatite Atopique), Dermatite Atopique, atopic dermatitis/eczema
Treatment Dupilumab
Clinical Study IdentifierNCT03667014
SponsorUniversity of California, San Francisco
Last Modified on10 August 2022

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