Clinical Trial

Pramipexole and the Risk of Serious Adverse Events

Completed
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Summary
This is a population-based cohort study assessing whether initiation of a higher dose of pramipexole (0.25 or 0.375 mg/day), compared with a lower dose (0.125 mg/day), in older adults with advanced chronic kidney disease (CKD) (an estimated glomerular filtration rate \[eGFR\] \<45 mL/min/1.73 m² but not receiving dialysis or having a history of kidney transplantation) is associated with a higher 30-day risk of a composite outcome of all-cause hospitalization or all-cause emergency visits, or all-cause mortality.
Trial Details
NCT Number NCT07382960
Lead Sponsor London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Conditions Older Adults (65 Years and Older), Chronic Kidney Disease (CKD)
Enrollment 1,100 participants
Start Date 2008-01-01
Primary Completion 2024-12-01 (estimated)
Study Completion 2024-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-02-03