Clinical Trial

Citalopram and the Risk of Serious Adverse Events

Completed
View on ClinicalTrials.gov →
Summary
This population-based cohort study aims to evaluate the safety of initiating a new outpatient prescription of citalopram at 20 mg/day (higher dose) compared to 10 mg/day (lower dose) in adults aged 65 years and older with reduced kidney function. The primary research question is whether initiating a higher dose of citalopram (20 mg/day) versus a lower dose (10 mg/day) in older adults with low kidney function (defined as an estimated glomerular filtration rate \[eGFR\] less than 45 mL/min per 1.73 m2, without dialysis or a history of kidney transplantation) is associated with an increased 30-day risk of a composite outcome comprising all-cause hospitalization, all-cause emergency department visits, or all-cause mortality.
Trial Details
NCT Number NCT07399795
Lead Sponsor London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Conditions Chronic Kidney Disease (CKD), Elderly, Outpatient
Enrollment 7,110 participants
Start Date 2008-01-01
Primary Completion 2025-01-01 (estimated)
Study Completion 2026-01 (estimated)
Updated on ClinicalTrials.gov 2026-02-10