Skip to content

Hidradenitis Suppurativa Prospective Observational Registry and Biospecimen Repository

Hidradenitis Suppurativa Prospective Observational Registry and Biospecimen Repository

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04115566
Acronym
HS PROGRESS
Enrollment
3000
Registered
2019-10-04
Start date
2020-08-01
Completion date
2035-05-01
Last updated
2026-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hidradenitis Suppurativa

Brief summary

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.

Interventions

None listed

Sponsors

University of California, San Francisco
Lead SponsorOTHER
UCB Pharma
CollaboratorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
10 Years to No maximum

Inclusion criteria

1. Male or female ≥ 10 years of age 2. Diagnosis of HS by a dermatologist or practitioner experienced in making a diagnosis of HS 3. 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.

Exclusion criteria

1\. Inability to give informed consent or unavailability of a parent/guardian who is able and willing to give informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Primary Objective2019-2035The primary aim of this study is to identify clinical and biologic characteristics of hidradenitis suppurativa.

Secondary

MeasureTime frameDescription
Secondary Objective2019-2035Secondary aims include correlating alterations in clinical and biological characteristics with disease status, and identifying genetic variants that predict disease progression or response to therapy.

Countries

United States

Contacts

CONTACTKaelin Chatterley
hsprogress@ucsf.edu415-961-3786
PRINCIPAL_INVESTIGATORHaley B Naik, MD, MHSc, FAAD

University of California, San Francisco

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026