drugset / Trial / NCT03251300

Mirabegron for Female OAB Patients: Comparison of Daytime and Nighttime Dosing

NCT03251300

Phase 4 Unknown 120 enrolled Far Eastern Memorial Hospital
RandomizedParallel-groupSingle-blindTreatment

Summary

The aim of this study is to elucidate whether night-time dosing of mirebegron can improve nocturia, compared with daytime dosing of mirabegron.

Timeline

Start
2017-08-01
Primary completion
2024-12-31
Completion
2024-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Mirabegron Other / unclassified 25 mg

Indications