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Search / Trial NCT05710393

Hidradenitis - an Analysis of Genetic Traits and Linkages in Families

Launched by UNIVERSITY OF CHICAGO · Jan 25, 2023

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

Hidradenitis Suppurativa Hs Acne Inversa Abscess Boils

ClinConnect Summary

This clinical trial is studying Hidradenitis Suppurativa (HS), a skin condition that causes painful lumps and sores. The researchers want to find out if there are genetic links or traits that connect people with HS to their family members. By understanding these connections, the hope is to discover the cause of HS and potentially find better treatments for it.

If you or someone in your family has HS and is between the ages of 25 and 56, you might be eligible to participate. The study is looking for both individuals with HS and their family members who do not have the condition. Unfortunately, children under 7 years old cannot take part. If you join the study, you can expect to share information about your health and family history, which could help researchers learn more about HS. This is an important step towards improving care and treatment options for everyone affected by this condition.

Gender

ALL

Eligibility criteria

  • 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

About University Of Chicago

The University of Chicago is a prestigious research institution renowned for its commitment to advancing medical science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, the University actively engages in cutting-edge research across various therapeutic areas. Its dedicated team of experienced investigators and state-of-the-art facilities enable the University of Chicago to conduct rigorous clinical studies aimed at improving patient outcomes and translating scientific discoveries into tangible healthcare solutions. The institution prioritizes ethical standards and patient safety, ensuring that all trials adhere to the highest regulatory guidelines and best practices in clinical research.

Locations

Chicago, Illinois, United States

Patients applied

HC

1 patients applied

Trial Officials

Peter Nagele, MD, MSc

Principal Investigator

University of Chicago Medicine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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