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Completed Phase 4 Interventional

Effect Of Detrol LA With Behavioral Intervention In Overactive Bladder Subjects Dissatisfied With Recent OAB Medication.

ClinicalTrials.gov ID: NCT00230789

Public ClinicalTrials.gov record NCT00230789. 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 Oct 21, 2026, 7:09 AM 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 Multicenter, Multiphase, Single Arm, Open Label Study To Evaluate The Effects Of Tolterodine ER In Conjunction With Behavioral Intervention On Subject Satisfaction And Over- Active Bladder Symptoms (Urgency Urinary Incontinence (UUI), Urgency, Frequency) In Overactive Bladder Subjects Who Were Dissatisfied With Their Most Recent Antimuscarinic OAB Medication Therapy.

Brief summary

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

To evaluate the effect of tolterodine ER in conjunction with behavioral intervention on subject satisfaction in OAB subjects who were dissatisfied with their most recent antimuscarinic OAB medication therapy.

Study identification

NCT ID
NCT00230789
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
417 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
Oct 2005 (Type not available)
Primary completion
Dec 2006 (Actual)
Completion
Dec 2006 (Actual)
Last update posted
Jan 27, 2021

2005 – 2006

United States locations

U.S. sites
51
U.S. states
22
U.S. cities
51
Facility City State ZIP Site status
Pfizer Investigational Site Phoenix Arizona — —
Pfizer Investigational Site Sun Lakes Arizona — —
Pfizer Investigational Site Little Rock Arkansas — —
Pfizer Investigational Site Beverly Hills California — —
Pfizer Investigational Site Buena Park California — —
Pfizer Investigational Site Mission Viejo California — —
Pfizer Investigational Site Modesto California — —
Pfizer Investigational Site Oceanside California — —
Pfizer Investigational Site Paramount California — —
Pfizer Investigational Site Sacramento California — —
Pfizer Investigational Site Torrance California — —
Pfizer Investigational Site Tustin California — —
Pfizer Investigational Site Colorado Springs Colorado — —
Pfizer Investigational Site Wheat Ridge Colorado — —
Pfizer Investigational Site Hallandale Florida — —
Pfizer Investigational Site Orlando Florida — —
Pfizer Investigational Site Wellington Florida — —
Pfizer Investigational Site Woodstock Georgia — —
Pfizer Investigational Site Libertyville Illinois — —
Pfizer Investigational Site Mattoon Illinois — —
Pfizer Investigational Site Newton Kansas — —
Pfizer Investigational Site Milford Massachusetts — —
Pfizer Investigational Site Manchester Missouri — —
Pfizer Investigational Site St Louis Missouri — —
Pfizer Investigational Site Westhampton New Jersey — —
Pfizer Investigational Site Albuquerque New Mexico — —
Pfizer Investigational Site Albany New York — —
Pfizer Investigational Site Endwell New York — —
Pfizer Investigational Site Garden City New York — —
Pfizer Investigational Site Poughkeepsie New York — —
Pfizer Investigational Site The Bronx New York — —
Pfizer Investigational Site Greensboro North Carolina — —
Pfizer Investigational Site Hickory North Carolina — —
Pfizer Investigational Site Raleigh North Carolina — —
Pfizer Investigational Site Canton Ohio — —
Pfizer Investigational Site Zanesville Ohio — —
Pfizer Investigational Site Norman Oklahoma — —
Pfizer Investigational Site Abington Pennsylvania — —
Pfizer Investigational Site Bala-Cynwyd Pennsylvania — —
Pfizer Investigational Site Camp Hill Pennsylvania — —
Pfizer Investigational Site Philadelphia Pennsylvania — —
Pfizer Investigational Site Williamsport Pennsylvania — —
Pfizer Investigational Site Mt. Pleasant South Carolina — —
Pfizer Investigational Site Simpsonville South Carolina — —
Pfizer Investigational Site Bartlett Tennessee — —
Pfizer Investigational Site Johnson City Tennessee — —
Pfizer Investigational Site New Tazewell Tennessee — —
Pfizer Investigational Site Houston Texas — —
Pfizer Investigational Site Provo Utah — —
Pfizer Investigational Site Mountlake Terrace Washington — —
Pfizer Investigational Site Spokane Washington — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00230789, 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 Jan 27, 2021 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00230789 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →