drugset / Trial / NCT02106182

Efficacy and Safety of Silodosin on Nocturia for Patients With Benign Prostatic Hyperplasia

NCT02106182

Phase 4 Completed 135 enrolled JW Pharmaceutical
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to determine safety and efficacy of silodosin, which is a treatment for benign prostatic hyperplasia with high selectivity to α1A-receptor, on patients with benign prostatic hyperplasia accompanied by nocturia.

Timeline

Start
2014-01-02
Primary completion
2016-03-02
Completion
2016-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Silodosin Unknown 8 mg Oral