Clinical Trials Directory

Trials / Completed

CompletedNCT00546637

Fesoterodine "add-on" Male Overactive Bladder Study

A Randomized, Double-Blind, Placebo-Controlled Study To Evaluate The Efficacy And Safety Of Fesoterodine As An "Add-On" Therapy In Men With Persistent Overactive Bladder Symptoms Under Monotherapy Of Alpha Blocker For Lower Urinary Tract Symptoms.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
947 (actual)
Sponsor
Pfizer · Industry
Sex
Male
Age
40 Years
Healthy volunteers
Not accepted

Summary

To evaluate the efficacy and safety of fesoterodine on overactive bladder symptom improvement when added to ongoing alpha blocker treatment.

Conditions

Interventions

TypeNameDescription
DRUGFesoterodineFesoterodine 4mg or 8mg
DRUGPlaceboPlacebo

Timeline

Start date
2007-11-01
Primary completion
2009-02-01
Completion
2009-02-01
First posted
2007-10-19
Last updated
2011-02-18
Results posted
2010-11-22

Locations

137 sites across 19 countries: United States, Belgium, Brazil, Canada, Colombia, Germany, Greece, India, Malaysia, Netherlands, Norway, Philippines, Poland, Singapore, Slovakia, South Korea, Spain, Sweden, Thailand

Source: ClinicalTrials.gov record NCT00546637. Inclusion in this directory is not an endorsement.

Fesoterodine "add-on" Male Overactive Bladder Study (NCT00546637) · Clinical Trials Directory