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Study identifier: NCT05403710 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingHS

Botulinum Toxin Therapy in Hidradenitis Suppurativa

Condition: Hidradenitis Suppurativa · Hyperhidrosis  ·  Sponsor: University of Massachusetts, Worcester

PhaseN/A
Planned participants20
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNoCheck eligibility criteria ↓
WhereWorcester, Massachusetts, United States

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

This study will build on data from mice and humans implicating TRPV1 nociceptors in the pathogenesis of the type-17 chronic inflammatory skin disease Hidradenitis Suppurativa (HS). In this study, the investigators will test the hypothesis that inhibiting neuropeptide activity with botulinum toxin reduces pathogenic inflammation.

This description comes directly from the study's public registry record.

Talk to the study team

Sarah K Whitley, MD PhD  ·  (508)856-4086  ·  sarah.whitley@umassmed.edu

Deborah White, Deborah Peduzzi  ·  (508)856-2664  ·  deborah.white@umassmed.edu

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion: * Adults between ages 18 and 75 years with established diagnosis of hidradenitis suppurativa (HS) * HS skin lesions of duration at least 1 year, HS skin lesions in at least two different body areas Exclusion: * Age \< 18 years or \> 75 years * pregnant or breastfeeding * neuromuscular disorder (ex. ALS, myasthenia gravis, Lambert-Eaton syndrome, myopathy) * medical co-morbidity that is a relative contraindication to skin biopsy procedure (ex. end stage congestive heart failure or coagulopathy) * active bacterial, fungal, or viral infection in the treatment area * known hypersensitivity to botulinum toxin A preparations or any of their components (human albumin, saline, lactose, sodium succinate) * prisoners * adults unable to consent for themselves.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

University of Massachusetts Chan Medical SchoolWorcester, Massachusetts, United StatesRecruiting

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Worcester

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