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NCT07316192Possibly a fitRecruiting

Comparing two wound dressings for hidradenitis suppurativa surgery

Hidradenitis Suppurativa (HS)

Part of Infections, Skin clinical trials.

This study compares two wound dressings used after surgery for hidradenitis suppurativa (HS) to see which one helps wounds heal better. It may help if you need a wide surgical excision for HS and can attend follow-up visits.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
10 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years or older and have a confirmed diagnosis of hidradenitis suppurativa that requires surgery to remove a large area of affected skin.
  • You can understand and sign a consent form in English.
  • You are willing and able to come to all scheduled follow-up appointments until the wound is ready for a second surgical closure.
  • You are not allergic to any of the wound dressing materials (polyvinyl alcohol), local anesthetics, or silver.
  • You do not have medical conditions that make lidocaine unsafe for you, such as certain heart problems.
  • You are not pregnant or breastfeeding.
  • You do not have severe immune system suppression (e.g., recent chemotherapy, organ transplant, uncontrolled HIV, or high-dose steroids).
  • Your diabetes is well-controlled (HbA1c of 10% or lower if tested in the last 3 months).
  • You do not have an active infection or sepsis at the time of surgery.
  • You can commit to all follow-up visits until the second stage of wound closure is complete.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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