Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07282782

A Prospective, Randomized Parallel Group Study of the Efficacy of Vancomycin Administered Through Intraarticular Injection Versus Intraosseous Injection Versus Intravenous Infusion in Patients Undergoing Total Knee Arthroplasty

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
University of California, San Diego · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Periprosthetic joint infection (PJI) is a national health crisis and leads to very poor outcomes for patients undergoing elective joint replacement. Within the realm of elective total knee arthroplasty (TKA), various methods of infection prophylaxis are in place. These include sterile precautions, would/tissue handling, and antibiotic prophylaxis. With respect to the latter, various approaches have been utilized including intravenous and intraosseous administration of vancomycin, preoperatively. Intraosseous administration does require another wound and a specific device to administer. We proposed that intraarticular injection of vancomycin is non-inferior to intraosseous administration, thus reducing wounds, time, and cost.

Conditions

Interventions

TypeNameDescription
DRUGVancomycinIntraosseous or Intraarticular administration of Vancomycin

Timeline

Start date
2024-06-10
Primary completion
2026-12-31
Completion
2028-12-31
First posted
2025-12-15
Last updated
2025-12-15

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07282782. Inclusion in this directory is not an endorsement.