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Behavior Enhances Drug Reduction of Incontinence (BE-DRI)
This study has been completed.
Sponsors and Collaborators: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Information provided by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ClinicalTrials.gov Identifier: NCT00090584
  Purpose

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.


Condition Intervention Phase
Urinary Incontinence
Drug: Tolterodine
Behavioral: Combination Drug (tolterodine) and Behavior Treatment
Phase II
Phase III

MedlinePlus related topics: Urinary Incontinence
Drug Information available for: Tolterodine Tolterodine tartrate
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Behavior Enhances Drug Reduction of Incontinence

Further study details as provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK):

Estimated Enrollment: 300
Study Start Date: August 2004
Estimated Study Completion Date: June 2006
  Eligibility

Ages Eligible for Study:   21 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion:

  • Female
  • Urge predominant incontinence
  • Incontinent > 3 mos
  • Available for 8 mos of followup

Exclusion:

  • Pregnancy or < 6 mos post-partum
  • Hypersensitivity to drug (tolterodine)
  • Systemic disease that affects bladder function (e.g., Parkinson's disease, MS, spinal cord injury)
  • History of extensive behavior treatment
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00090584

Locations
United States, Alabama
University of Alabama
Birmingham, Alabama, United States, 35233
United States, California
University of California
San Diego, California, United States, 92103
United States, Illinois
Loyola University Medical Center
Maywood, Illinois, United States, 60153
United States, Maryland
University of Maryland
Baltimore, Maryland, United States, 21201
United States, Michigan
Oakwood Hospital and Medical Center
Royal Oak, Michigan, United States, 48123
United States, Pennsylvania
University of Pittsburgh
Pittsburgh, Pennsylvania, United States, 15213
United States, Texas
University of Texas Southwestern
Dallas, Texas, United States, 75390
University of Texas Health Sciences Center
San Antonio, Texas, United States, 78229
United States, Utah
University of Utah
Salt Lake City, Utah, United States, 84132
Sponsors and Collaborators
Investigators
Study Chair: William D Steers, M.D. University of Virginia
  More Information

www.uitn.net  This link exits the ClinicalTrials.gov site

Publications indexed to this study:
Responsible Party: NIDDK ( Debuene Chang, MD Project Officer )
Study ID Numbers: BE-DRI
Study First Received: August 27, 2004
Last Updated: December 21, 2007
ClinicalTrials.gov Identifier: NCT00090584  
Health Authority: United States: Federal Government

Keywords provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK):
Urge urinary incontinence
Drug/Behavior treatment

Study placed in the following topic categories:
Signs and Symptoms
Urologic Diseases
Urination Disorders
Urinary Incontinence
Urinary Incontinence, Urge
Tolterodine

Additional relevant MeSH terms:
Muscarinic Antagonists
Urological Manifestations
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Cholinergic Antagonists
Physiological Effects of Drugs
Cholinergic Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 14, 2009