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Completed Not applicable Interventional Accepts healthy volunteers Results available

Behavior Enhances Drug Reduction of Incontinence (BE-DRI)

ClinicalTrials.gov ID: NCT00090584

Public ClinicalTrials.gov record NCT00090584. 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, 10:59 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

Behavior Enhances Drug Reduction of Incontinence

Brief summary

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

The primary aim of this study is to test if the addition of behavioral treatment to drug therapy for the treatment of urge incontinence will increase the number of patients who can discontinue drug therapy and sustain a significant reduction of incontinence.

Study identification

NCT ID
NCT00090584
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Carelon Research
Other
Enrollment
307 participants

Conditions and interventions

Interventions

Drug · Behavioral

Eligibility (public fields only)

Age range
21 Years and older
Sex
Female
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Aug 2004 (Type not available)
Primary completion
Dec 2005 (Actual)
Completion
Aug 2006 (Actual)
Last update posted
Jun 17, 2013

2004 – 2006

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35233 —
University of California San Diego California 92103 —
Loyola University Medical Center Maywood Illinois 60153 —
University of Maryland Baltimore Maryland 21201 —
Oakwood Hospital and Medical Center Royal Oak Michigan 48123 —
University of Pittsburgh Pittsburgh Pennsylvania 15213 —
University of Texas Southwestern Dallas Texas 75390 —
University of Texas Health Sciences Center San Antonio Texas 78229 —
University of Utah Salt Lake City Utah 84132 —

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 NCT00090584, 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 Jun 17, 2013 · Synced Oct 21, 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 NCT00090584 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →