drugset / Trial / NCT00234546

Asian Botulinum Clinical Trial Designed for Early Stroke Spasticity

NCT00234546 ↗

Phase 4 Completed 162 enrolled Ipsen
RandomizedParallel-groupDouble-blindTreatment

Summary

The aim of this clinical study is to investigate the efficacy and safety of Dysport® in patients with early onset of upper limb spasticity within 2-12 weeks after stroke.

Timeline

Start
2003-02
Primary completion
—
Completion
2007-10

Outcome

Met primary endpoint

paper At 4 weeks postinjection, BoNT-A significantly improved MAS scores. PMID 22371239 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin type A Protein / enzyme biologic 500 iu Other

Indications