Global cross-sectional burden-of-illness study in adolescent and adult patients with atopic dermatitis (MEASURE-AD)
- Conditions
- L20-L30Dermatitis and eczema
- Registration Number
- DRKS00019854
- Lead Sponsor
- AbbVie Deutschland GmbH & Co. KG
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 1593
• physician confirmed diagnosis of atopic dermatitis
• moderate to severe AD patients who are (i) current candidates for systemic therapy for AD according to the HCP, or (ii) currently receiving systemic therapy for AD.
• medication history available within the last 6 months
• able to understand the questionnaires, with parental support as required for adolescents
• willing to provide a patient authorization form to use and disclose personal health information (or informed consent, where applicable) to participate in the study; for adolescent subjects, authorization and/or consent will be provided by a parent or legal guardian, where applicable
Patients will be excluded if currently participating in interventional clinical trial(s). Participation in another non-interventional study or registry does not exclude a patient from this study.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To characterize the multidimensional burden of disease in adolescent and adult patients with moderate to severe AD with single data collection
- Secondary Outcome Measures
Name Time Method • To describe the patient characteristics, current local treatment patterns and the treatment history of moderate to severe AD patients in dermatology offices and clinics.<br>• To characterize disease burden related to pain, sleep and mental health in patients with moderate to severe AD.<br>• To evaluate work productivity and out of pocket costs for AD patients<br>• To characterize health care resource utilization.<br>• To assess the impact of chronic comorbidities on disease burden.<br>• To evaluate the frequency and characteristics of patients with inadequately controlled disease receiving different treatments.<br>• To evaluate the frequency and characteristics of patients who experience AD flare.