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Completed Phase 3 Interventional Results available

Clinical Trial to Evaluate the Efficacy and Safety of Fesoterodine in Comparison to Tolterodine for Overactive Bladder (OAB)

ClinicalTrials.gov ID: NCT00444925

Public ClinicalTrials.gov record NCT00444925. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 2, 2026, 12:52 PM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

12-Week, Randomized, Double-Blind, Double-Dummy,Placebo-Controlled, Parallel-Group, Multicenter Trial To Evaluate The Efficacy And Safety Of Fesoterodine In Comparison To Tolterodine ER In Patients With Overactive Bladder (OAB)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To evaluate the efficacy and safety of fesoterodine in comparison to tolterodine and placebo for overactive bladder

Study identification

NCT ID
NCT00444925
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
1,712 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2007 (Type not available)
Primary completion
Jul 2008 (Actual)
Completion
Jul 2008 (Actual)
Last update posted
Mar 24, 2015

2007 – 2008

United States locations

U.S. sites
41
U.S. states
27
U.S. cities
39
Facility City State ZIP Site status
Pfizer Investigational Site Homewood Alabama 35209 —
Pfizer Investigational Site Huntsville Alabama 35801 —
Pfizer Investigational Site Mobile Alabama 36608 —
Pfizer Investigational Site Carmichael California 95608 —
Pfizer Investigational Site Orangevale California 95662 —
Pfizer Investigational Site San Diego California 92103-6204 —
Pfizer Investigational Site Aurora Colorado 80012 —
Pfizer Investigational Site Waterbury Connecticut 06708 —
Pfizer Investigational Site Miami Florida 33186 —
Pfizer Investigational Site Wellington Florida 33414 —
Pfizer Investigational Site Atlanta Georgia 30342 —
Pfizer Investigational Site Coeur d'Alene Idaho 83814 —
Pfizer Investigational Site Sandpoint Idaho 83864 —
Pfizer Investigational Site Aurora Illinois 60504 —
Pfizer Investigational Site West Des Moines Iowa 50266 —
Pfizer Investigational Site Newton Kansas 67114 —
Pfizer Investigational Site Shrevport Louisiana 71106 —
Pfizer Investigational Site Watertown Massachusetts 02472 —
Pfizer Investigational Site Chaska Minnesota 55318 —
Pfizer Investigational Site Lawrenceville New Jersey 08648 —
Pfizer Investigational Site Albuquerque New Mexico 87109 —
Pfizer Investigational Site Garden City New York 11530 —
Pfizer Investigational Site Mineola New York 11501 —
Pfizer Investigational Site Burlington North Carolina 27215 —
Pfizer Investigational Site Concord North Carolina 28025 —
Pfizer Investigational Site Huntersville North Carolina 28078 —
Pfizer Investigational Site Dayton Ohio 45439 —
Pfizer Investigational Site Allentown Pennsylvania 18103 —
Pfizer Investigational Site Allentown Pennsylvania 18106 —
Pfizer Investigational Site Pittsburgh Pennsylvania 15212 —
Pfizer Investigational Site Pittsburgh Pennsylvania 15213-3180 —
Pfizer Investigational Site East Providence Rhode Island 02914 —
Pfizer Investigational Site Charleston South Carolina 29425 —
Pfizer Investigational Site Columbia South Carolina 29201 —
Pfizer Investigational Site Kingsport Tennessee 37660 —
Pfizer Investigational Site Milan Tennessee 38358 —
Pfizer Investigational Site Houston Texas 77024 —
Pfizer Investigational Site Provo Utah 84604 —
Pfizer Investigational Site Chesapeake Virginia 23320 —
Pfizer Investigational Site Seattle Washington 98104 —
Pfizer Investigational Site Menomonee Falls Wisconsin 53051 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 137 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00444925, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 24, 2015 · Synced Nov 2, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00444925 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →