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Completed Phase 3 Interventional Results available

Study of Topically Administered Oxybutynin Gel in Patients With Urge Incontinence

ClinicalTrials.gov ID: NCT00909181

Public ClinicalTrials.gov record NCT00909181. 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 22, 2026, 12:24 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 Double-Blind, Randomized, Parallel, Placebo-Controlled, Multicenter Study Evaluating the Effect of Treatment With Topically Administered Oxybutynin Gel in Patients With Urinary Frequency, and Urge and Mixed Urinary Incontinence With a Predominance of Urge Incontinence Episodes With an Open-Label Extension

Brief summary

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

The primary objective of the double-blind phase of the study is to compare the effects of two doses of oxybutynin gel to placebo gel. The objective of the open-label extension is to evaluate the extended safety and skin-irritation profile of topically administered oxybutynin gel. The hypothesis is that topically administered oxybutynin gel will decrease (compared to placebo) the number of incontinence episodes per week, average daily urinary frequency, and urinary urgency; increase average urinary void volume; and improve patient quality of life.

Study identification

NCT ID
NCT00909181
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Antares Pharma Inc.
Industry
Enrollment
626 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
Mar 2009 (Type not available)
Primary completion
Jul 2010 (Actual)
Completion
Nov 2010 (Actual)
Last update posted
Jul 2, 2014

2009 – 2010

United States locations

U.S. sites
55
U.S. states
26
U.S. cities
53
Facility City State ZIP Site status
Not listed Birmingham Alabama 35233 —
Not listed Little Rock Arkansas 72211 —
Not listed Laguna Hills California 92653 —
Not listed Los Angeles California 90048 —
Not listed San Diego California 92103 —
Not listed San Diego California 92120 —
Not listed Farmington Connecticut 06032 —
Not listed New Britain Connecticut 06052 —
Not listed New Port Richey Florida 34625 —
Not listed North Miami Florida 33161 —
Not listed Pembroke Pines Florida 33024 —
Not listed Sarasota Florida 34232 —
Not listed St. Petersburg Florida 33710 —
Not listed Tampa Florida 33607 —
Not listed Wellington Florida 33414 —
Not listed Columbus Georgia 31904 —
Not listed Sandy Springs Georgia 30328 —
Not listed Stockbridge Georgia 30281 —
Not listed Evanston Illinois 60201 —
Not listed West Des Moines Iowa 50266 —
Not listed Shreveport Louisiana 71106 —
Not listed Annapolis Maryland 21401 —
Not listed Towson Maryland 21204 —
Not listed Watertown Massachusetts 02472 —
Not listed Grand Rapids Michigan 49503 —
Not listed Saginaw Michigan 48604 —
Not listed Chesterfield Missouri 63017 —
Not listed Las Vegas Nevada 89130 —
Not listed Brooklyn New York 11211 —
Not listed Endwell New York 13760 —
Not listed Kingston New York 12401 —
Not listed Poughkeepsie New York 12601 —
Not listed Williamsville New York 14221 —
Not listed Cary North Carolina 27518 —
Not listed Charlotte North Carolina 28209 —
Not listed Harrisburg North Carolina 28075 —
Not listed Raleigh North Carolina 27607 —
Not listed Raleigh North Carolina 27609 —
Not listed Salisbury North Carolina 28144 —
Not listed Wilmington North Carolina 28401 —
Not listed Winston-Salem North Carolina 27103 —
Not listed Wadsworth Ohio 44218 —
Not listed Bethany Oklahoma 73008 —
Not listed Corvallis Oregon 97330 —
Not listed Bala-Cynwyd Pennsylvania 19004 —
Not listed Landsdale Pennsylvania 19446 —
Not listed Greenville South Carolina 29615 —
Not listed Mt. Pleasant South Carolina 29464 —
Not listed Myrtle Beach South Carolina 29572 —
Not listed Sioux Falls South Dakota 57104 —
Not listed Fayetteville Tennessee 37334 —
Not listed Provo Utah 84604 —
Not listed Richmond Virginia 23294 —
Not listed Seattle Washington 98104 —
Not listed Spokane Washington 99207 —

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 NCT00909181, 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 Jul 2, 2014 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00909181 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →