drugset / Trial / NCT02244294

FLOMAX® Versus Placebo, in Male Patients With Acute Urinary Retention Related to Benign Prostatic Hyperplasia (BPH)

NCT02244294

Phase 2 Completed 176 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

To establish whether the administration of FLOMAX® improves the outcome of a trial without catheter (TWOC) after an episode of acute urinary retention and to determine whether spontaneous voiding is maintained over the course of six months of active treatment

Timeline

Start
2001-03
Primary completion
2005-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Tamsulosin Other / unclassified 0.4 mg