Expired Study
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Indianapolis, Indiana


Purpose:

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


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


NCT ID:

NCT00651690


Primary Contact:

Study Director
Medical Director
Allergan


Backup Contact:

N/A


Location Contact:

Indianapolis, Indiana
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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