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PERmixon® in LUTS Evaluation Study (PERLES) — PERLES  

Benign Prostatic Hyperplasia (BPH) Clinical Trial

Official title:
PERMIXON® 160 mg Hard Capsule Versus Placebo in the Treatment of Symptomatic Lower Urinary Tract Symptoms Due to Benign Prostatic Hyperplasia

Clinical Trial Summary

The aim of this study is to support the efficacy of Permixon 160 mg b.i.d. in treating subjects with symptomatic Benign Prostatic Hyperplasia (BPH), compared to placebo, using Tamsulosine LP 0.4 mg as a reference treatment.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02121613
Study type Interventional
Source Pierre Fabre Medicament
Contact
Status Completed
Phase Phase 4
Start date April 2014
Completion date June 2016
View Details
See also
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