Actively Recruiting

Phase Not Applicable
Age: 18Years - 89Years
MALE
Healthy Volunteers
ID06464770

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

Age: 18Years - 89Years
MALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • English speaking
  • Male
  • Aged 18 to 89 years
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

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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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