Study to Assess Impact of Dysport Injections Early After Stroke on Upper Limb Spasticity Progression

PHASE4CompletedINTERVENTIONAL
Enrollment

42

Participants

Timeline

Start Date

December 31, 2014

Primary Completion Date

March 31, 2016

Study Completion Date

March 31, 2016

Conditions
StrokeUpper Limb Spasticity
Interventions
BIOLOGICAL

Botulinum toxin type A

Subjects to receive Dysport® 500U administered intramuscularly in the targeted upper limb.

DRUG

Placebo

Placebo administered intramuscularly in the targeted upper limb.

Trial Locations (4)

1003

Center for Neurodiagnostic and Therapeutic Services Metropolitan Medical Center, Manila

10700

Department of rehabilitation Medicine Faculty of medicine Siriraj Hospital, Madihol University Hospital, Bangkok

59100

Neurology Laboratory -University Malaya Medical Centre, Kuala Lumpur

569766

TTSH Rehabilitation Centre Ang Mo Kio Community Hospital, Singapore

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Ipsen

INDUSTRY