Hidradenitis Suppurativa (HS) Tunneling Wounds

  • STATUS
    Recruiting
  • End date
    Mar 1, 2023
  • participants needed
    15
  • sponsor
    University of Miami
Updated on 25 May 2022

Summary

The purpose of this study is to look at the change in the microbiome (bacterial composition) of an HS tunneling wound and examine if treatment with an antibiofilm surfactant wound gel (ABWG) (a topical medication that will fight bacteria attached to the surface of those tunnels) changes the bacterial composition of the wounds.

Details
Condition Hidradenitis Suppurativa
Treatment antibiofilm surfactant wound gel (ABWG)
Clinical Study IdentifierNCT04648631
SponsorUniversity of Miami
Last Modified on25 May 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Adults 18 years old and older
Have diagnosis of HS confirmed by a dermatologist
Have at least one HS related tunneling wound that is at least 2 centimeters in length
Able to provide informed consent

Exclusion Criteria

Individuals who are not yet adults
Women known to be pregnant
Prisoners
Subjects, who in the opinion of the PI, cannot comply with home application of the treatment
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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