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Completed Phase 4 Interventional Results available

Safety and Efficacy Study of Transdermal Oxybutynin to Treat Overactive Bladder With a Neurological Condition

ClinicalTrials.gov ID: NCT00224016

Public ClinicalTrials.gov record NCT00224016. 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 Jul 22, 2026, 3:24 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 Multi-Center, Open-Label (OL), Active-Controlled, Dose-Titration Study Evaluating the Safety, Efficacy and PK of Oxybutynin Transdermal Systems in the Treatment of Detrusor Overactivity in Pediatric Patients

Study identification

NCT ID
NCT00224016
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Watson Pharmaceuticals
Industry
Enrollment
57 participants

Conditions and interventions

Interventions

  • Oxybutynin Drug

Drug

Eligibility (public fields only)

Age range
6 Years to 15 Years
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
Nov 30, 2004
Primary completion
Mar 31, 2007
Completion
Aug 31, 2008
Last update posted
Feb 8, 2012

2004 – 2008

United States locations

U.S. sites
23
U.S. states
16
U.S. cities
23
Facility City State ZIP Site status
Watson Investigational Site Little Rock Arkansas
Watson Investigational Site Orange County California
Watson Investigational Site San Diego California
Watson Investigational Site Denver Colorado
Watson Investigational Site Washington D.C. District of Columbia
Watson Investigational Site Detroit Michigan
Watson Investigational Site Minneapolis Minnesota
Watson Investigational Site Jackson Mississippi
Watson Investigational Site Kansas City Missouri
Watson Investigational Site St Louis Missouri
Watson Investigational Site Voorhees Township New Jersey
Watson Investigational Site Albany New York
Watson Investigational Site Buffalo New York
Watson Investigational Site Poughkeepsie New York
Watson Investigational Site Ashville North Carolina
Watson Investigational Site Durham North Carolina
Watson Investigational Site Columbus Ohio
Watson Investigational Site Oklahoma City Oklahoma
Watson Investigational Site Hershy Pennsylvania
Watson Investigational Site Dallas Texas
Watson Investigational Site Houston Texas
Watson Investigational Site Plano Texas
Watson Investigational Site Salt Lake City Utah

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 NCT00224016, 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 Feb 8, 2012 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00224016 live on ClinicalTrials.gov.

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