drugset / Trial / NCT01302938

Web-based Methodology Trial to Evaluate the Efficacy and Safety of Tolterodine ER in Subjects With Overactive Bladder

NCT01302938 ↗

Phase 4 Terminated 18 enrolled Viatris Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

To compare the effect of tolterodine ER 4 mg to placebo on patient reported outcomes in subjects with overactive bladder after 1, 4, and 12 weeks of treatment using an innovative web-based trial design

Timeline

Start
2011-03
Primary completion
2012-08
Completion
2012-08

Outcome

Outcome not reported

Stopped (Enrollment): “Stop date for randomization: 31/5/2012. Recruitment terminated due to lack of recruitment. No new safety issues were identified.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Tolterodine Unknown 4 mg Oral

Indications