Study to Evaluate Safety, Efficacy of Botulinum Toxin Type A in Patients With Cervical Dystonia
Completed · Phase 2 · Has a placebo group
Conditions studied: Cervical Dystonia
In brief
Study is to investigate the use of the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) scale in a cervical dystonia population treated with botulinum toxin type A, and placebo.
Key facts
- Study ID
- NCT00564681
- Run by
- Allergan
- People needed
- 242
- Starts
- 2007-12-01
- Expected to finish
- 2009-12-01
- Last updated by the study team
- 2016-01-05
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of cervical dystonia
You may not qualify if…
- Current or previous botulinum toxin treatment of any type for any condition
Where it is running
- Study site — Winston-Salem, North Carolina, United States
- Study site — Halifax, Nova Scotia, Canada
- Study site — Prague, Czechia
- Study site — Berlin, Germany
- Study site — Budapest, Hungary
- Study site — Mumbai, India
- Study site — Manila, Philippines
- Study site — Warsaw, Poland
- Study site — Moscow, Russia
- Study site — Belgrade, Serbia
- Study site — Singapore, Singapore
- Study site — Spisska Nova, Slovakia
- Study site — Cape Town, South Africa
- Study site — Tainan, Taiwan
- Study site — Bangkok, Thailand
- Study site — Bristol, United Kingdom
Full record on ClinicalTrials.gov
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