About this trial
HS is relatively common in the United States with a prevalence of 0.1-1.0%. 1 HS has a dramatic impact on quality of life, significantly more so than other chronic skin diseases, such as psoriasis or atopic dermatitis (AD). HS also has a large economic impact, due to frequent emergency department and inpatient care utilization, and re-hospitalization rates similar to congestive heart failure. Unfortunately, few treatment options are effective. There are currently three FDA-approved treatments for HS, including adalimumab, secukinumab, and bimekizumab, each with only 40- 60% respond to treatment and over 50% lose response within one year . The overarching goal of this pilot study is to investigate the central hypothesis that oral microbiota transplant therapy(MTT) alters the gut microbiome in patients with Hidradenitis Suppurativa (HS), influencing cutaneous microbiota via systemically absorbed gut-derived metabolites.
Eligibility criteria
Qualifiers
Able and willing to provide informed consent
English speaking
Age >= 18years of age
Diagnosis of hidradenitis suppurativa by a dermatologist
Disqualifiers
Non-English speaking
Refusal or inability to provide informed consent
Planning on moving within 6 months from start of study
Allergy to neomycin or vancomycin
Trial design
Treatments tested in this trial
- Fecal Microbiota - lyophilized
- Placebo drug