Actively Recruiting
Multi-Country, Cross-sectional Study to Characterize Real World Burden of Disease in Adolescent and Adult Patients With Alopecia Areata, Vitiligo or Hidradenitis Suppurativa MEASURE AAVitHS
Led by AbbVie · Updated on 2026-02-13
2795
Participants Needed
116
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the impact and burden of three skin conditions moderate or severe alopecia areata, non-segmental vitiligo, and moderate to severe hidradenitis suppurativa. The study includes adolescents and adults and aims to understand how these conditions affect quality of life and daily functioning in a large global population. This is an observational study where participants with each condition will have a single visit for data collection following routine clinical practice. No experimental treatments are given instead, the study gathers information during this one visit to assess disease characteristics and impact. During the visit, participants will complete questionnaires and clinical assessments specific to their condition. These include tools measuring symptom impact, hair loss severity, skin depigmentation, and quality of life related to each disease. This helps researchers better understand the real-world burden of these conditions. Participation involves only this one visit, with no long-term follow-up or additional procedures.
CONDITIONS
Brief Title
A Real World Study to Globally Assess Disease Burden in Adolescent and Adult Participants With Alopecia Areata, Vitiligo, or Hidradenitis Suppurativa
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants with physician-confirmed diagnosis of non-segmental vitiligo, moderate to severe alopecia areata, or moderate to severe hidradenitis suppurativa
- Participants aged 12 years or older
- Ability to understand study questionnaires, with caregiver support as needed for adolescents
You will not qualify if you...
- Participating in interventional clinical trial(s) at time of study visit
- Unable or unwilling to comply with study requirements and patient-reported outcome collection
Research Team
B
Beth Rycroft
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