Optimizing Infection Prophylaxis Prior to Shoulder Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18-89
SponsorUniversity of Washington

About this trial

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 criteria

Qualifiers

English speaking

Disqualifiers

Self report very sensitive skin

Allergic to chlorhexidine

Used antibiotics in the last three months

Used acne treatment in the last three months

Trial design

Treatments tested in this trial

  • Chlorhexidine Gluconate

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators