Clinical Trials Directory

Trials / Terminated

TerminatedNCT00821184

Behavioral Modification and Vesicare Versus Vesicare Alone for Urge Incontinence in Patients With Overactive Bladder

A Prospective Randomized Trial of Behavioral Modification and Solifenacin (Vesicare)vs Solifenacin (Vesicare) Alone for the Treatment of Urge Incontinence in Patients With an Overactive Bladder

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Lahey Clinic · Academic / Other
Sex
Female
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This study will help determine if behavior modification performed in conjunction with oral Vesicare anticholinergic therapy is more effective for treating overactive bladder symptoms than oral Vesicare anticholinergic therapy alone.

Detailed description

Overactive bladder symptoms are commonly treated with oral anticholinergic medications that work by stopping muscles from tightening or behavioral modification. This study will help determine if behavior modification (fluid regulation, pelvic exercises, timed voiding) performed in conjunction wth oral Vesicare anticholinergic therapy, is more effective for treating overactive bladder symptoms than oral Vesicare anticholinergic therapy alone.

Conditions

Interventions

TypeNameDescription
DRUGVesicare (solifenacin)5mg po qd
BEHAVIORALVesicare (solifenacin) plus behavioral modification5 mg dose po once daily plus behavioral modification

Timeline

Start date
2006-09-01
Primary completion
2008-09-01
Completion
2008-09-01
First posted
2009-01-13
Last updated
2018-04-04
Results posted
2010-07-30

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00821184. Inclusion in this directory is not an endorsement.