ClinicalTrials.Veeva

Menu

Hidradenitis - an Analysis of Genetic Traits and Linkages in Families

The University of Chicago logo

The University of Chicago

Status

Enrolling

Conditions

Hidradenitis Suppurativa

Study type

Observational

Funder types

Other

Identifiers

NCT05710393
IRB18-1861

Details and patient eligibility

About

The aim of this study is to find a genetic link or family trait connecting persons with Hidradenitis Suppurativa (HS) to each other. As a result, discover the cause and perhaps treatment for Hidradenitis Suppurativa (HS).

Full description

Hidradenitis suppurativa (HS) is a chronic, debilitating skin disease characterized by multiple abscesses located predominantly in areas such as armpit, genital, pelvic, and perineum. It is considered an orphan disease of unknown origin and no existing treatment with a population prevalence estimated between 1-4%. It develops in otherwise healthy patients after puberty and affects patients life-long. HS often requires multiple surgical procedures to drain large abscesses, or hospitalization to treat infected wounds, can lead to feelings of personal embarrassment and social stigmatization.

Anecdotal evidence from affected families shows that HS often "runs in families" and may be inherited in a Mendelian fashion; however, no adequately powered study has been undertaken to investigate this hypothesis. This project aims to characterize the inheritance pattern of HS in families, and identify the genetic cause of this disease in those families with evidence for monogenic inheritance.

Data collection includes blood sample analysis (DNA), medical history, and information pertaining to any known family history of HS, from which a familial pedigree can be generated. This 'family-based' genetic study design will include both affected and unaffected family members, ideally spanning several generations. Therefore, study patients will be asked to refer their immediate and extended (affected and unaffected) family members to this research study.

Enrollment

500 estimated patients

Sex

All

Ages

7+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants (affected) with Hidradenitis Suppurativa and related symptoms
  • Family (unaffected) of participants with Hidradenitis Suppurativa

Exclusion criteria

  • Children under 7-years of age

Trial design

500 participants in 2 patient groups

Affected
Description:
(Affected) persons with a medical history of symptoms related to Hidradenitis Suppurativa.
Unaffected-control
Description:
(Unaffected) family of participants, having no history of symptoms related to Hidradenitis Suppurativa.

Trial contacts and locations

1

Loading...

Central trial contact

Frank Brown Jr

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems