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
| Type | Name | Description |
|---|---|---|
| DRUG | trospium chloride | Sanctura XR® (trospium chloride) 60 mg once daily on an empty stomach for 14 weeks |
| DRUG | placebo | Placebo 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.