Actively Recruiting
Augmented Renal Clearance in Neurocritical Care
Led by University of Alberta · Updated on 2026-02-18
512
Participants Needed
3
Research Sites
260 weeks
Total Duration
On this page
Sponsors
U
University of Alberta
Lead Sponsor
U
University of Kentucky
Collaborating Sponsor
AI-Summary
What this Trial Is About
Stroke, severe brain injury, uncontrolled seizures and brain infections are the most common life-threatening neurological illnesses in the world with an estimated combined annual hospital management cost of up to 44 billion dollars. Seizures and infections are common complications following acute neurological illnesses and contribute significantly to poor outcomes if not promptly treated with appropriately dosed anti-seizure medications and antibiotics, respectively. Limited research suggested that many of those patients present with a phenomenon called augmented renal clearance (ARC) or, in other words, enhanced kidney function. ARC may have a significant influence on how medications are removed from the body potentially resulting in insufficient doses and treatment failure. Therefore, patients with ARC require higher medication doses; however, ARC is largely undetected using kidney assessment methods currently used in practice. In addition, it is not clear how medications should be dosed in those with ARC. The majority of ARC research has not focused on patients with life-threatening neurological illnesses. Thus, clinicians are likely under-dosing vital medications in those patients, and completely unaware. There is an immediate need to address the gap in knowledge. Therefore, this research aims to characterize the phenomenon of ARC in patients with life-threatening neurological illnesses through identifying the frequency, duration, contributing factors and clinical impact of ARC. Adult patients admitted to the neurosciences intensive care unit for life-threatening neurological illnesses will be enrolled in the study. Urine and blood samples wil be collected from participants to determine the presence of ARC and identify its contributing factors. In addition, blood samples will be collected from participants treated with select antibiotics and anti-seizure medications to determine their concentration and propose dose adjustment in those with ARC. This research is expected to improve the care of patients with life-threatening neurological illnesses through efficient identification and monitoring of patients exhibiting ARC facilitating timely medication dosage optimization. Furthermore, recommendations of optimal doses of commonly used medications in patients with ARC would improve the likelihood of treatment success with potential to improve patients' health and wellbeing.
CONDITIONS
Official Title
Augmented Renal Clearance in Neurocritical Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-85 years
- Admitted to ICU at one of the participating sites
- Diagnosis of 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 allow urine collection
You will not qualify if you...
- Incarceration
- Expected ICU stay less than 72 hours, which is not enough time for monitoring
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
UK HealthCare
Lexington, Kentucky, United States, 40536
Actively Recruiting
2
The Ohio State University Wexner Medical Center
Columbus, Ohio, United States, 43210
Actively Recruiting
3
University of Alberta Hospital
Edmonton, Alberta, Canada, T6G 2X8
Actively Recruiting
Research Team
S
Sherif H Mahmoud, BSc (Pharm), MSc, PhD, FNCS
CONTACT
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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