drugset / Trial / NCT05931276

CSP #2026 - Beta Blocker Dialyzability on Cardiovascular Outcomes

NCT05931276

Phase 3 Recruiting 2540 enrolled VA Office of Research and Development
RandomizedParallel-groupOpen-labelTreatment

Summary

The investigators aim to determine, using a point-of-care randomized controlled trial design, if hemodialysis patients, who are randomized to metoprolol succinate (a dialyzable, beta-1 selective beta blocker), have an improved cardiovascular outcome compared to those randomized to carvedilol (a non-dialyzable, non-selective beta blocker with alpha-1 antagonist properties). The investigators will also examine intervention practices to identify components that best support engagement and sustainability.

Timeline

Start
2024-05-22
Primary completion
2026-12-31
Completion
2028-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Carvedilol Other / unclassified 3.125 mg
Comparator Carvedilol Other / unclassified 6.25 mg
Comparator Carvedilol Other / unclassified 12.5 mg
Comparator Carvedilol Other / unclassified 25 mg
Comparator Metoprolol Other / unclassified 12.5 mg
Comparator Metoprolol Other / unclassified 25 mg
Comparator Metoprolol Other / unclassified 50 mg
Comparator Metoprolol Other / unclassified 100 mg
Comparator Metoprolol Other / unclassified 200 mg