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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00090584
Study type Interventional
Source New England Research Institutes
Contact
Status Completed
Phase N/A
Start date August 2004
Completion date August 2006

See also
  Status Clinical Trial Phase
Completed NCT02758561 - Motivational Interviewing in Women`s Pelvic Wellness Education N/A