drugset / Trial / NCT00234546
Asian Botulinum Clinical Trial Designed for Early Stroke Spasticity
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Botulinum toxin type A | Protein / enzyme biologic | 500 iu | Other |