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Clinical Trial Summary

The purpose of this study is to evaluate swallowing efficiency in patients with cervical dystonia following treatment with botulinum toxin Type A.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01384214
Study type Interventional
Source Allergan
Contact
Status Completed
Phase Phase 4
Start date October 2008
Completion date June 2009

See also
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Recruiting NCT05317390 - Clinical Validation of DystoniaNet Deep Learning Platform for Diagnosis of Isolated Dystonia N/A
Completed NCT01655862 - A Prospective, Observational Study of Patients With Cervical Dystonia (Dystonie) Treated With OnabotulinumtoxinA N/A
Completed NCT01056861 - Effects of Botulinum Toxin in Cervical Dystonia N/A
Withdrawn NCT00175604 - Comparative Trial of Botox in the Management of Children With Congenital Muscular Torticollis Phase 1