About this trial
Hidradenitis suppurativa (HS) is a common and debilitating skin disease that is poorly understood and understudied. As a result, little is known about disease prognosis and few effective treatments exist for this condition. This prospective observational cohort study aims to comprehensively characterize the clinical and biological features of HS. The results of this research will provide a basis for the development of an HS clinical classification system and identification of potential treatments for HS.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Male or female ≥ 10 years of age
Diagnosis of HS by a dermatologist or practitioner experienced in making a diagnosis of HS
Written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study.
Disqualifiers
None
Trial population
HS Patients
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Primary Objective
The primary aim of this study is to identify clinical and biologic characteristics of hidradenitis suppurativa.
Secondary outcomes
Secondary Objective
Secondary aims include correlating alterations in clinical and biological characteristics with disease status, and identifying genetic variants that predict disease progression or response to therapy.
Sponsors and contacts
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University of California, San Francisco
Lead sponsor
UCB Pharma
Collaborator