Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Fluorescent Probe for Assessment of Renal Elimination

Accurate measures of kidney function is important for precision dosing of many medications. The current methods of determining kidney function largely hinge on the use of equations that use common laboratory values such as serum creatinine \& static variables like age \& weight. These are helpful for trending over time, but often are inaccurate during times of medical illness. Other more accurate methods of measuring kidney function include urine collection, although this is not commonly used because of various reasons that make the collection inconvenient or unreliable. The new transdermal glomerular filtration (tGFR) device permits accurate, real-time evaluation of kidney function. This novel method has not been rigorously compared with urine collection \& other methods of determining kidney function in hospitalized patients. The goal of the study is to compare tGFR with other accepted methods of determining kidney function.

Participants needed: 200
Trial details
Phase: Phase 4Age: 18-65Biological sex: AllType: InterventionalSponsor: Aaron CookUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

18-65 years old [+2]

Prisoners [+2]

Status: Recruiting

Telavancin Blood and Cerebrospinal Fluid Concentrations in Patients With External Ventricular Drainage

The proposed study aims to evaluate the CNS penetration of telavancin in a critically ill population using cerebrospinal fluid (CSF) drawn from external ventricular drains (EVDs). Patients with EVDs were chosen as the target population because they frequently require prolonged admission to the intensive care unit and drainage of CSF in order to prevent hydrocephalus. The estimated sample size is 20 subjects. This is a prospective cohort of patients with SAH. Patients will be included if they have an in-dwelling EVD, aged 18-85 years old. Subjects will receive telavancin 10mg/kg (maximum 1000mg) every 24 hours for 3 consecutive doses. Serial serum and CSF samples will be obtained. An 8-hour urine collection will be completed on study day 2 in order to define the patient's measured creatinine clearance.

Participants needed: 20
Trial details
Phase: Phase 4Age: 18-85Biological sex: AllType: InterventionalSponsor: Aaron CookUpdated: Dec 26, 2025Locations: 1
Eligibility criteria

Adult aged 18-85 years [+1]

history of hypersensitivity to telavancin or similar agents [+4]