Actively Recruiting

Phase Not Applicable
Age: 18Years - 89Years
MALE
Healthy Volunteers
NCT06464770

Optimizing Infection Prophylaxis Prior to Shoulder Surgery

Led by University of Washington · Updated on 2024-12-05

40

Participants Needed

1

Research Sites

173 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

CONTACT

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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