Behavior Enhances Drug Reduction of Incontinence (BE-DRI)
Completed · Not applicable
Conditions studied: Urinary Incontinence (UI)
In brief
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.
Key facts
- Study ID
- NCT00090584
- Run by
- Carelon Research
- People needed
- 307
- Starts
- 2004-08-01
- Expected to finish
- 2006-08-01
- Last updated by the study team
- 2013-06-17
Who can join
Age: 21 and older. Sex: female. Healthy volunteers: accepted.
Where it is running
- University of Alabama — Birmingham, Alabama, United States
- University of California — San Diego, California, United States
- Loyola University Medical Center — Maywood, Illinois, United States
- University of Maryland — Baltimore, Maryland, United States
- Oakwood Hospital and Medical Center — Royal Oak, Michigan, United States
- University of Pittsburgh — Pittsburgh, Pennsylvania, United States
- University of Texas Southwestern — Dallas, Texas, United States
- University of Texas Health Sciences Center — San Antonio, Texas, United States
- University of Utah — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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