RecruitingNot ApplicableNCT06464770

Optimizing Infection Prophylaxis Prior to Shoulder Surgery


Sponsor

University of Washington

Enrollment

40 participants

Start Date

Aug 31, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this interventional study is to determine the amount of skin C. acnes reduction with increased pressure during the chlorhexidine gluconate, brand name ChloraPrep, application. The main question it aims to answer is: Does changing the pressure applied during the ChloraPrep application impact the amount of C. acnes bacteria on the skin after one hour? Researchers will compare ChloraPrep applied at a pressure similar to a gentle wipe to ChloraPrep applied at a pressure similar to a massage to see if wash the amount of C. acnes on the skin after one hour is different. Participants will have one shoulder washed with ChloraPrep using pressure meant to impact the dermal layer, similar to a gentle wipe, and the other shoulder washed with ChloraPrep using pressure meant to impact the subdermal layer, similar to a massage. Participants will have swabs taken of their skin before the ChloraPrep application and again one hour after application to look for the amount of C. acnes on the skin.


Eligibility

Sex: MALEMin Age: 18 YearsMax Age: 89 Years

Inclusion Criteria1

  • English speaking

Exclusion Criteria5

  • Self report very sensitive skin
  • Allergic to chlorhexidine
  • Used antibiotics in the last three months
  • Used acne treatment in the last three months
  • Wounds on your shoulders

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Interventions

DRUGChlorhexidine Gluconate

Test Group: the participant's shoulder skin will be treated by the study team with the standard chlorhexidine wash at lower pressure (similar to a gentle wipe) for 30 seconds Control Group: the participant's shoulder skin will be treated by the study team with the standard chlorhexidine wash at higher pressure (similar to a massage) for 30 seconds


Locations(1)

University of Washington

Seattle, Washington, United States

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NCT06464770


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