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A Study of an Investigational Study Drug for Benign Prostatic Hyperplasia (0906-140)

Phase 3
Completed
Conditions
Benign Prostatic Hyperplasia
Registration Number
NCT00127179
Lead Sponsor
Organon and Co
Brief Summary

The purpose of this trial is to determine the efficacy and safety of an investigational drug in patients with benign prostatic hyperplasia.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
600
Inclusion Criteria
  • Patients with benign prostatic hyperplasia
Exclusion Criteria
  • Patients who are suspected to be suffering from prostatic cancer

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change from baseline in the International Prostate Symptom Score
Secondary Outcome Measures
NameTimeMethod
Change from baseline in Prostate volume
Change from baseline in maximum urinary flow rate, %
Change from baseline in QOL - index
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