Clinical and Biological Characteristics of Hidradenitis Suppurativa
1 other identifier
observational
1,000
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2016
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 15, 2016
CompletedFirst Submitted
Initial submission to the registry
May 27, 2019
CompletedFirst Posted
Study publicly available on registry
May 30, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 15, 2026
May 4, 2026
April 1, 2026
10 years
May 27, 2019
April 28, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
The primary aim of this study is to identify clinical and biologic characteristics of hidradenitis suppurativa.
2016-2026
Secondary Outcomes (1)
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.
2016-2026
Study Arms (2)
Hidradenitis Suppurativa Patients
Patients with physician diagnosed Hidradenitis Suppurativa
Healthy Volunteers
Healthy volunteers without any skin conditions or recent history of antibiotic use.
Eligibility Criteria
Patients with Hidradenitis Suppurativa
You may qualify if:
- Age 13 years or older
- Diagnosis of HS clinically-confirmed by a physician
You may not qualify if:
- \. Inability to give informed consent or have a parent/guardian who is able and willing to give informed consent.
- Healthy Volunteer
- No history of chronic skin conditions
- No recent history of antibiotic use
- \. Inability to give informed consent or have a parent/guardian who is able and willing to give informed consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of California, San Francisco
San Francisco, California, 94115, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Haley B Naik, MD, MHSc, FAAD
University of California, San Francisco
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 10 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 27, 2019
First Posted
May 30, 2019
Study Start
July 15, 2016
Primary Completion (Estimated)
July 15, 2026
Study Completion (Estimated)
July 15, 2026
Last Updated
May 4, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share