Clinical Trials Directory

Trials / Completed

CompletedNCT01313767

MEDITOXIN® Versus BOTOX® in the Treatment of Post-stroke Spasticity of the Upper Limb Spasticity

A Randomized, Double Blind, Multi-center, Active Drug Controlled Clinical Trial to Compare the Efficacy and Safety of MEDITOXIN® Versus BOTOX® in Treatment of Post Stroke Upper Limb Spasticity

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
196 (actual)
Sponsor
Medy-Tox · Industry
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

This study is a randomized, double blind, multi-center, active drug controlled, phase III clinical trial to compare the efficacy and safety of MEDITOXIN® versus BOTOX® in treatment of post stroke upper limb(wrist, finger, thumb) spasticity Approximately 196 subjects(1:1 group ratio)will be enrolled. Subjects will receive a single treatment of intramuscular Investigational product up to 360U. The subjects will be observed every 4 weeks until 12 weeks post injection. Outcome measures include Modified Ashworth Scale (MAS), Disability Assessment Scale (DAS), Global Assessment Scale(patient or caregiver/investigator) and Carer burden scale. The primary efficacy endpoint is the change from baseline at week 4 for wrist flexor muscle tone as measured on the Modified Ashworth Scale. Safety parameters will also be measured including adverse events, vital signs and clinical laboratory tests (haematology, serum chemistry and urinanalysis).

Detailed description

Each completed subject will attend 4\~5 clinic visits. The maximum study duration is 15 weeks. Only one upper limb (eligible inclusion/exclusion criteria) will be injected and evaluated in the study. Maximun injection dose is 360U.

Conditions

Interventions

TypeNameDescription
DRUGBotulinum toxin type ABotulinum toxin type A
DRUGBotulinum Toxin type ABotulinum Toxin type A

Timeline

Start date
2011-03-01
Primary completion
2012-01-01
Completion
2012-02-01
First posted
2011-03-14
Last updated
2019-03-29
Results posted
2019-03-29

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01313767. Inclusion in this directory is not an endorsement.