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Not yet recruiting Not applicable NCT07283068

IO Vancomycin Into the Medial Malleolus vs IV Administration in Revision TKA

No applicable phase (e.g. observational)
Conditions: Revision Total Knee Arthroplasty

Sponsor: The Methodist Hospital Research Institute

trial.available_in: БГ
Overview
Purpose of this study is to compare the efficacy of intravenous and intraosseous antibiotic administration techniques during revision total knee arthroplasty
Who can participate
Inclusion Criteria: * Patient is undergoing a revision total knee arthroplasty where in the opinion of the investigator, the patient's existing tibial component excludes the tibial tubercle as a valid intraosseous injection site. * Patient is able to understand the study design and intervention and gives informed consent to participate in the study. * Age \> 18 years. Exclusion Criteria: * Contraindication to receiving vancomycin, cefepime, ancef, or other standard of care pre-operative antibiotic (allergy, medical issue, etc). * Patient received or is scheduled to receive intravenous Vancomycin within 7 days prior to their planned revision procedure. * Any hardware, condition, or anatomic status that prevents the medial malleolus from being a viable intraosseous injection site. * Refusal to participate * Any condition, in the opinion of the primary investigator, that deems the participant unsuitable for participation in the research study.
Interventions
Intraosseous Vancomycin
DRUG
Locations

Location information is not available.

Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
15.06.2026
Completion date
15.06.2030
Registry ID
NCT07283068
Source
clinicaltrials.gov
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