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Study identifier: NCT06999161 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Therapeutic Drug Monitoring of Beta-lactams and Renal Hyperclearance in Patients Admitted to Intensive Care for Acute Brain Injury

Condition: Critical Illness · Brain Injuries  ·  Sponsor: Centre Hospitalier Universitaire de Nīmes

PhaseN/A
Planned participants140
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Augmented Renal Clearance (ARC), defined as a supraphysiological increase in renal function, is frequently observed in critically ill patients, particularly those with acute brain injury. ARC complicates the management of renally eliminated drugs, specifically beta-lactam antibiotics, by enhancing drug clearance and thereby increasing the risk of underdosing and therapeutic failure. Although pharmacological therapeutic drug monitoring (TDM) is recommended to optimize dosing, it remains limited by issues of accessibility, highlighting the need for alternative approaches to identify at-risk patients and adjust dosing based on renal function. Early identification of patients at risk for subtherapeutic beta-lactam plasma concentrations could enable timely dose adjustments. A combined assessment of renal function and beta-lactam TDM could enhance our understanding of the kinetics of both parameters. These data may support the development of predictive models capable of proposing individualized dosing regimens based on renal function. Optimizing beta-lactam plasma concentrations in this patient population could improve infection management and potentially enhance clinical outcomes.

This description comes directly from the study's public registry record.

Talk to the study team

Claire ROGER, MD, pHD  ·  +33 466683331  ·  claire.roger@chu-nimes.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU de Nîmes - Hôpital Universitaire CarémeauNîmes, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06999161