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  3. Dysport 222
Research Study

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 Stothers

Overview

Body Locations and Systems
Urinary Incontinence
Multiple Sclerosis
Spinal Cord Injury
ClinicalTrials.gov#
NCT02660138
Status
Recruiting
Start/End Dates
Nov 29, 2016
Locations
ICORD – Blusson Spinal Cord Centre
Name/Title
Ivy Allard, Research Nurse
Phone
604-875-4111 ext.69876
Email Address
ivy.allard@vch.ca
Purpose 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

Visit ClinicalTrials.gov for more information. 

Disclaimer

Study Coordinators and Research Nurses cannot give medical advice over the phone. Telephone numbers and email addresses are provided for obtaining additional information on specific research studies only. If you have specific questions which require clinical expertise, please call your primary care physician.

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