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0.05% Chlorhexidine Gluconate for Periprosthetic Joint Infection
N/A
Waitlist Available
Research Sponsored by University of Southern California
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients presenting to Keck Hospital of USC or USC Verdugo Hills Hospital for primary total knee arthroplasty or total hip arthroplasty.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 90 days
Awards & highlights
Study Summary
This trial will compare the rates of microbial contamination on surgical instruments placed in three different types of surgical splash basins: those filled with sterile water, 3.5% betadine, or 0.05% CHG. The overall purpose of the study is to investigate the efficacy of 0.05% CHG and determine if it is an appropriate solution to use in surgical splash basins for joint replacement surgeries.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 90 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~90 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Microbial Contamination Rate of Surgical Instruments
Secondary outcome measures
90-Day Wound Complication
Trial Design
3Treatment groups
Experimental Treatment
Group I: Sterile WaterExperimental Treatment1 Intervention
Group II: 3.5% betadineExperimental Treatment1 Intervention
Group III: 0.05% chlorhexidine gluconateExperimental Treatment1 Intervention
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Who is running the clinical trial?
University of Southern CaliforniaLead Sponsor
906 Previous Clinical Trials
1,596,258 Total Patients Enrolled
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