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Clinical Trial

Post-incision Antimicrobial Wash vs C. Acnes in Shoulder Arthroplasty

NCT: NCT06831422 · RECRUITING

NCT IDNCT06831422
StatusRECRUITING
Start Date2025-05-05
Completion2027-12
SponsorHenry Ford Health System (OTHER)
First posted
Last updated

Brief Summary

The purpose of this randomized controlled trial is to determine the effect of post-incision wash using various novel antimicrobial solutions on the rate of positive C. Acnes cultures collected from adults undergoing primary shoulder replacement surgery. Subjects will be randomly assigned in a 1:1:1:1 fashion to groups that will receive one of the following treatments: * Post-incision application of Xperience Antimicrobial wash (NextScience, Jacksonville, FL) * Post-incision application of 3% hydrogen peroxide * Post-incision application of 10% povidone-iodine (betadine) * No post-incision treatment (control) The investigators hypothesize that the subjects treated with the antimicrobial solutions after initial incision will have lower rates of positive C. Acnes cultures. The investigators also hypothesize that post-incision application of Xperience Antimicrobial wash and Betadine will have an equal reduction in the incidence of C. acnes as Hydrogen Peroxide.

Frequently Asked Questions

What is Post-incision Antimicrobial Wash vs C. Acnes in Shoulder Arthroplasty?

Post-incision Antimicrobial Wash vs C. Acnes in Shoulder Arthroplasty is a clinical trial registered under NCT06831422. Current status: RECRUITING.

What is the status of NCT06831422?

The current status of NCT06831422 (Post-incision Antimicrobial Wash vs C. Acnes in Shoulder Arthroplasty) is: RECRUITING.

When did Post-incision Antimicrobial Wash vs C. Acnes in Shoulder Arthroplasty start?

Post-incision Antimicrobial Wash vs C. Acnes in Shoulder Arthroplasty started on 2025-05-05.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.