drugset / Trial / NCT06954129

A Pragmatic Clinical Trial Comparing the Risk of Acute Kidney Injury During Treatment With Vancomycin and Piperacillin-Tazobactam vs. Vancomycin and Cefepime in Hospitalized Patients

NCT06954129

Phase 4 Recruiting 750 enrolled University of Pennsylvania
RandomizedParallel-groupOpen-labelTreatment

Summary

Hospitalized patients with suspected or confirmed infection are commonly treated with vancomycin (VN) in combination with either piperacillin-tazobactam (PT) or cefepime (CP). Although these regimens have similar effectiveness, recent observational evidence suggests they may differ in terms of the risk for acute kidney injury (AKI). Interpretation of existing evidence is complicated by the limitations of creatinine, the standard biomarker used to monitor kidney function, which has poor sensitivity and specificity for drug induced AKI. To address this important knowledge gap, the investigators propose to conduct a pragmatic, open-label, non-inferiority trial that will examine the comparative risk of AKI between these standard-of-care antibiotic combinations using sensitive and specific markers of drug-induced AKI. We hypothesize that the regimen of VN in combination with PT (VN+PT) is noninferior to the regimen of VN in combination with CP (VN+CP) in terms of AKI risk.

Timeline

Start
2026-01-28
Primary completion
2029-05
Completion
2029-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Amoxicillin Other / unclassified 2.25 g Intravenous
Comparator Amoxicillin Other / unclassified 4.5 g Intravenous
Comparator Cefepime Small molecule 500 mg Intravenous
Comparator Cefepime Small molecule 1000 mg Intravenous
Comparator Cefepime Small molecule 2000 mg Intravenous
Comparator Vancomycin Other / unclassified Intravenous

Indications