A Phase III, Multicentre, Randomised, Double Blind, Parallel Group, Placebo Controlled Study To Assess The Efficacy And Safety Of One Or More Intradetrusor Treatments Of 600 Or 800 Units of Dysport® For The Treatment Of Urinary Incontinence In Subjects With Neurogenic Detrusor Overactivity Due To Spinal Cord Injury Or Multiple Sclerosis
Principal Investigator
Lynn StothersOverview
Study Start/End
Nov 29, 2016 to Jul 25, 2017Locations
Diamond Health Care Centre, ICORD – Blusson Pavilion
Name/Title
Ivy Allard, Research NursePhone
604-875-4111 ext.69876Email Address
ivy.allard@vch.caPurpose of Study
The purpose of this study is to provide confirmatory evidence of the safety and efficacy of two Dysport® (AbobotulinumtoxinA) doses (600 units [U] and 800 U), compared to placebo in reducing urinary incontinence (UI) in adult subjects treated for neurogenic detrusor overactivity (NDO) due to spinal cord injury (SCI) or multiple sclerosis (MS).
Eligibility
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Disclaimer
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