NCT01505439

A Study to Estimate the Efficacy and Safety of Solifenacin in Female With Stress Urinary Incontinence and Urgency Urinary Incontinence

A Prospective, Open Label, Single Arm, Multicenter Study to Estimate the Efficacy and Safety of Solifenacin in Female With Clinically Significant Stress Urinary Incontinence and Urgency Urinary Incontinence

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 311 (actual)
• Sponsor: Jeong Gu Lee · Academic / Other
• Sex: Female
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This study is to investigate the effects of solifenacin on urgency urinary incontinence symptoms and incontinence quality-of-life (I-QoL) in female patients with clinically significant stress urinary incontinence accompanied by urgency urinary incontinence.

Conditions

• Stress Urinary Incontinence
• Urgency Urinary Incontinence

Interventions

Type	Name	Description
DRUG	solifenacin	oral

Timeline

• Start date: 2011-06-01
• Primary completion: 2014-06-01
• Completion: 2014-06-01
• First posted: 2012-01-06
• Last updated: 2016-06-15

Locations

6 sites across 1 country: South Korea