Clinical Trial

Model-Informed Precision Dosing on Amikacin and Vancomycin Therapy in Critically Ill Children

Completed
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Summary
Achieving optimal antibiotic exposure in critically ill pediatric patients is difficult due to (their) dynamic physiology and variability. Conventional weight-based regimens often fail to reach pharmacokinetic/pharmacodynamic (PK/PD) targets for narrow therapeutic index agents such as vancomycin and amikacin. Model-Informed Precision Dosing (MIPD), which integrates Bayesian forecasting with population pharmacokinetics (popPK), offers a potentially valuable yet underexplored approach in pediatric intensive care to better attain and sustain target exposure. This pilot randomized clinical trial evaluated MIPD-guided dosing of vancomycin and amikacin using InsightRX Nova® versus standard of care (SoC) in a tertiary PICU. Patients whose model-recommended doses matched standard regimens were analyzed under SoC. Primary outcomes included prediction accuracy (a priori vs a posteriori) and model fit; secondary outcomes assessed dose optimization, inflammatory response, renal safety, treatment duration, and mortality.
Trial Details
NCT Number NCT07315438
Lead Sponsor Hacettepe University
Conditions Model Informed Precision Dosing
Enrollment 41 participants
Start Date 2023-12-01
Primary Completion 2025-08-30 (estimated)
Study Completion 2025-10-27 (estimated)
Updated on ClinicalTrials.gov 2026-01-02