Phase
Condition
Acne Inversa
Rosacea
Scalp Disorders
Treatment
Fecal Microbiota - lyophilized
Placebo drug
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Able and willing to provide informed consent
English speaking
Age >= 18years of age
Diagnosis of hidradenitis suppurativa by a dermatologist
Women who are not post-menopausal (at least 12 months of non-therapy inducedamenorrhea) or surgically sterile (e.g. absence of ovaries and/or uterus) mustremain abstinent or use a highly effective form of birth control (e.g. oralcontraception, transdermal patch, barrier, intrauterine device). Periodic abstinenceand early withdraw are not acceptable methods
Able to comply to study measures in the opinion of the investigator.
Stable doses of all medications for 30 days prior to baseline
Exclusion
Exclusion Criteria:
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
Anaphylactic food allergies
Pregnancy, breastfeeding or planning pregnancy during study period (negativepregnancy test needed for persons of childbearing potential)
Use of any topical or oral antibiotics within 30 days of randomization
Use of any oral antibiotics within 90 days of randomization
History of inflammatory bowel disease
Extensive bowel resection (e.g., subtotal colectomy, substantial removal of smallbowel)
No major bowel surgery within 4 weeks prior to baseline or planned major surgeryduring the study period
No active skin disease other than HS that could interfere with assessments
Study Design
Connect with a study center
University of Minnesota
Minneapolis, Minnesota 55414
United StatesActive - Recruiting
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