Studying Enhanced Kidney Clearance in Adults with Serious Brain Illnesses
in Neuroscience Intensive Care Units
Led by University of Alberta · Updated on 2026-02-18
512
Participants Needed
3
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Stroke, severe brain injury, status epilepticus, and meningitis are serious neurological illnesses that often lead to seizures and infections, causing poor patient outcomes if not treated properly. This research focuses on a condition called augmented renal clearance ARC, where kidney function is enhanced, affecting how medications are cleared from the body. The study aims to better understand ARC in patients with life-threatening neurological illnesses to improve medication dosing and treatment success.
The study is a multicenter prospective observational design involving adult patients admitted to Neuroscience Intensive Care Units with severe neurological conditions like intracerebral hemorrhage, subarachnoid hemorrhage, ischemic stroke, status epilepticus, meningitis, and traumatic brain injury. Participants will have their kidney function measured daily through urine collection for up to 10 days or until ICU discharge. Blood samples will be collected from patients receiving certain anti-seizure and antibiotic medications to measure drug levels and suggest dose adjustments for those with ARC.
During the study, researchers will collect urine and blood samples to detect ARC and its contributing factors. They will track kidney clearance and drug concentrations during hospital stays. The primary measures include creatinine clearance over 10 days or until ICU discharge and drug concentration after consistent dosing. This work aims to provide guidelines for identifying ARC and optimizing medication dosing to improve outcomes for patients with critical neurological illnesses.
CONDITIONS
Brief Title
Augmented Renal Clearance in Neurocritical Care
Research Team
S
Sherif H Mahmoud, BSc (Pharm), MSc, PhD, FNCS
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Admitted to an intensive care unit at a participating site
Diagnosed with subarachnoid hemorrhage, traumatic brain injury, intracerebral hemorrhage, meningitis, status epilepticus, or ischemic stroke
Provided informed consent
Foley catheter in place at time of consent to facilitate urine collection
You will not qualify if you...
Currently incarcerated
Expected intensive care unit stay is less than 72 hours due to insufficient monitoring time
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Monitoring
Duration - Up to 10 days or until ICU discharge
Participants are monitored daily for up to 10 days or until discharge from the intensive care unit with urine collection to measure creatinine clearance and blood sampling to determine drug concentrations.
Daily visits for urine collection and blood sampling
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Published Research Related To This Trial
Meropenem and piperacillin/tazobactam prescribing in critically ill patients: does augmented renal clearance affect pharmacokinetic/pharmacodynamic target attainment when extended infusions are used?
The importance of empiric antibiotic dosing in critically ill trauma patients: Are we under-dosing based on augmented renal clearance and inaccurate renal clearance estimates?
Jeffrey F Barletta, Alicia J Mangram, Marilyn Byrne...
Augmented renal clearance in the ICU: results of a multicenter observational study of renal function in critically ill patients with normal plasma creatinine concentrations*.