Actively Recruiting
Optimizing Infection Prophylaxis Prior to Shoulder Surgery Using Different Pressures of Chlorhexidine Gluconate Application
Led by University of Washington · Updated on 2024-12-05
40
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating how different pressures applied during the use of chlorhexidine gluconate (ChloraPrep) affect the amount of Cutibacterium acnes (C. acnes) bacteria on the skin. The study focuses on male adults aged 18 to 89 years who are preparing for shoulder surgery, aiming to determine if pressure similar to a gentle wipe versus a massage changes bacterial reduction one hour after application. Participants will have one shoulder washed with ChloraPrep using a gentle wiping pressure aimed at the dermal layer, and the other shoulder washed using a firmer massage-like pressure targeting the subdermal layer. Each application lasts 30 seconds. The study is randomized so that either the right or left shoulder receives the test or control treatment, allowing comparison between the two methods. During the study, skin swabs will be taken before and one hour after the application to measure the number of bacterial growth quadrants on culture plates. Researchers will monitor the reduction of C. acnes on each shoulder. Participants will be observed only during the application and follow-up swabbing, with no masking or blinding involved. The study will continue until the end of 2027, and participants' safety and bacterial levels will be closely tracked throughout.
CONDITIONS
Brief Title
Optimizing Infection Prophylaxis Prior to Shoulder Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- English speaking
- Male
- Aged 18 to 89 years
You will not qualify if you...
- Very sensitive skin
- Allergy to chlorhexidine
- Use of antibiotics in the last three months
- Use of acne treatment in the last three months
- Wounds on the shoulders
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single treatment visit
Participants receive chlorhexidine gluconate application on both shoulders with different pressures to evaluate infection prophylaxis prior to shoulder surgery.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
University of Washington
Seattle, Washington, United States, 98105
Actively Recruiting
Research Team
A
Anastasia Whitson
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
2
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