Clinical Trials Directory

Trials / Completed

CompletedNCT01089751

Efficacy of Sanctura XR (Trospium Chloride) for Reducing Overactive Bladder Symptoms in Female Subjects Refractory to Detrol LA (Tolterodine Tartrate Extended Release) Daily

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
322 (actual)
Sponsor
Allergan · Industry
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study will investigate the safety and efficacy of Sanctura XR (trospium chloride) daily in reducing urgency, urinary frequency and urinary urge incontinence in female patients with incontinence refractory to Detrol LA (tolterodine tartrate extended release) 4 mg therapy.

Conditions

Interventions

TypeNameDescription
DRUGtrospium chlorideSanctura XR® (trospium chloride) 60 mg once daily on an empty stomach for 14 weeks
DRUGplaceboPlacebo once daily on an empty stomach for 14 weeks.

Timeline

Start date
2010-03-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2010-03-19
Last updated
2013-09-26
Results posted
2013-09-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01089751. Inclusion in this directory is not an endorsement.