Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT04388163

Gentian Violet Treatment for Hidradenitis Suppurativa

Effects of Gentian Violet Treatment on Patients With Hidradenitis Suppurativa

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Wake Forest University Health Sciences · Academic / Other
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Not accepted

Summary

This is a survey study being conducted to describe how subjects with Hidradenitis suppurativa (HS) respond to treatment with gentian violet. The study will rely primarily on qualitative survey responses and quantitative changes in skin appearance.

Detailed description

Hidradenitis suppurativa (HS) is a chronic disease of the folliculopilosebaceous unit, often found in intertriginous areas of the body. The pain and impairment of HS leads patients to report a decreased quality of life, even in comparison to other debilitating cutaneous disease states. Pharmalogic management of HS can vary from topical antibiotics or intralesional corticosteroids for mild cases to immunosuppressants and biologic agents in refractory cases. Gentian violet is a topical antiseptic used to treat many cutaneous yeast infections. It also has a role in improving wound healing in sites of active ulceration. It is our hypothesis that gentian violet will help minimize skin trauma in sites of active HS to promote improved wound healing and quality of life.

Conditions

Interventions

TypeNameDescription
DRUGGentian VioletGentian violet is a topical antiseptic used to treat many cutaneous yeast infections. It also has a role in improving wound healing in sites of active ulceration.

Timeline

Start date
2025-08-01
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2020-05-14
Last updated
2025-09-04

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04388163. Inclusion in this directory is not an endorsement.