CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 14,000 enrolled
Drug / intervention
Tamsulosindrug
Likely dose
Tamsulosin 0.4 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT07274228
NCT07274228N/ACompleted

Risk of Serious Adverse Events Associated With Tamsulosin Use in Older Adults With Advanced Chronic Kidney Disease: A Population-Based Cohort Study Research Protocol

In Brief

An observational study evaluating Tamsulosin for Chronic Kidney Disease (CKD). Completed, enrolled 14,000 participants across 1 site.

Detailed Summary

This is a population-based cohort study assessing whether initiating a higher dose of tamsulosin (0.8 mg/day) compared to a lower dose (0.4 mg/day) in older adults with advanced chronic kidney disease (CKD) (an estimated glomerular filtration rate (eGFR) \<45 mL/min per 1.73 m² but not receiving dialysis or having a history of kidney transplantation) is associated with a higher 90-day risk of a composite outcome of all-cause hospitalization or all-cause emergency visits or all-cause mortality.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesCanada
Collaborators--

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 10, 2025
Enrollment StartJan 1, 2008
Primary CompletionDec 1, 2024
Study CompletionMar 1, 2025
TodayJul 2, 2026
Enrollment to primary: 16.9 yearsPosted 7 months ago

Interventions

Tamsulosindrug

The primary exposure of interest will be oral tamsulosin at a dose of 0.4 mg/day, representing the median dose in high-throughput computing analyses. For the primary comparison, oral tamsulosin at a dose of 0.4 mg/day will be chosen to reduce the influence of indication bias.