Study of Responsiveness of Seven Functional Tasks in Patients With Poststroke Upper Limb Spasticity With Botulinum Toxin Type A Treatment

Study Identifier
191622-065
CT.gov Identifier
NCT00651690
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Study Details

Medical Condition
  • Stroke
  • Movement Disorders - Other
    • Study Drug
  • Botulinum Toxin Type A
  • Placebo
    • Phase
    Phase 2
    Sex
    Female & Male
    Age
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Medically stable poststroke with focal unilateral upper-limb spasticity
    Exclusion Criteria:
    * Stroke within 6 months of the study enrollment visit * Previous or current botulinum toxin therapy of any type in the study limb

    Protocol Summary

    This study evaluates the responsiveness of 7 functional tasks to botulinum toxin Type A treatment in poststroke patients with spasticity of the upper-limb flexors

    Study Locations

    Location
    Status
    Location
    Indianapolis, Indiana, United States
    Status
    Not applicable