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Completed Phase 3 Interventional Results available

A Clinical Trial To Assess Fesoterodine On Treatment Satisfaction And Symptom Improvement In Overactive Bladder Patients

ClinicalTrials.gov ID: NCT00425100

Public ClinicalTrials.gov record NCT00425100. 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 May 14, 2026, 8:13 PM EDT

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

Official title

A 12-Week, Multicenter, Open-Label, Single-Arm Study To Evaluate The Effects Of Fesoterodine On Treatment Satisfaction And Symptom Relief In Overactive Bladder Patients.

Study identification

NCT ID
NCT00425100
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
516 participants

Conditions and interventions

Interventions

  • fesoterodine fumarate Drug

Drug

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
Dec 31, 2006
Primary completion
Sep 30, 2007
Completion
Sep 30, 2007
Last update posted
Dec 4, 2018

2007

United States locations

U.S. sites
24
U.S. states
19
U.S. cities
23
Facility City State ZIP Site status
Pfizer Investigational Site Homewood Alabama 35209
Pfizer Investigational Site Huntsville Alabama 35801
Pfizer Investigational Site La Mesa California 91942
Pfizer Investigational Site Orangevale California 95662
Pfizer Investigational Site Aurora Colorado 80012
Pfizer Investigational Site West Palm Beach Florida 33407
Pfizer Investigational Site Aurora Illinois 60504
Pfizer Investigational Site Pratt Kansas 67124
Pfizer Investigational Site Shreveport Louisiana 71106
Pfizer Investigational Site Milford Massachusetts 01757
Pfizer Investigational Site Omaha Nebraska 68114
Pfizer Investigational Site Woodlane New Jersey 08060
Pfizer Investigational Site Kingston New York 12401
Pfizer Investigational Site New York New York 10016
Pfizer Investigational Site Poughkeepsie New York 12601
Pfizer Investigational Site Winston-Salem North Carolina 27103
Pfizer Investigational Site Cincinnati Ohio 45212
Pfizer Investigational Site Bethany Oklahoma 73008
Pfizer Investigational Site Eugene Oregon 97401
Pfizer Investigational Site Sellersville Pennsylvania 18960
Pfizer Investigational Site Houston Texas 77024
Pfizer Investigational Site Salt Lake City Utah 84107
Pfizer Investigational Site Salt Lake City Utah 84124
Pfizer Investigational Site Milwaukee Wisconsin 53209

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 36 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00425100, 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 Dec 4, 2018 · Synced May 14, 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 protocol, eligibility criteria, and contact information for NCT00425100 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →