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Propiverine in Children Suffering From Non-Neurogenic Overactive Bladder and Urinary Incontinence

Urinary Incontinence Clinical Trial

Official title:
Treatment With Propiverine in Children Suffering From Non-Neurogenic Overactive Bladder and Urinary Incontinence: Results of a Randomized Placebo-Controlled Phase III Clinical Trial

Clinical Trial Summary

The study was conducted between 2004 and 2006 to prove efficacy and tolerability of the antimuscarinic propiverine compared to placebo in children suffering from non-neurogenic overactive bladder and urinary incontinence.

Clinical Trial Description

This clinical trial showed superior efficacy of propiverine over placebo and convincing tolerability for the treatment of children suffering from OAB and urinary incontinence. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00603343
Study type Interventional
Source APOGEPHA Arzneimittel GmbH
Contact
Status Completed
Phase Phase 3
Start date June 2004
Completion date December 2006
View Details
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