Observational Study of Botox® Treatment for Patients With Upper Limb Adult Spasticity

Study Identifier
MAF/AGN/NS/SPA/018
CT.gov Identifier
NCT01387074
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
  • Movement Disorders - Other
    • Study Drug
  • botulinum toxin Type A
    • Phase
    N/A
    Sex
    Female & Male
    Age
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Adult patients with upper limb spasticity following a stroke * Eligible to receive botulinum toxin Type A * No previous botulinum toxin Type A therapy
    Exclusion Criteria:
    * None

    Protocol Summary

    This is a prospective, non-interventional, observational study to collect data on the use of botulinum toxin Type A in a routine setting in patients with upper limb adult spasticity.

    Study Locations

    Location
    Status
    Location
    Itzehoe, Schleswig-Holstein, Germany
    Status
    Not applicable