Observational study to determine the type of patient with cervical dystonia that responds best to botulinum toxin treatment

Not Applicable

Completed

• Conditions: Idiopathic Cervical Dystonia; Neurological - Other neurological disorders

• Registration Number: ACTRN12609000800224
• Lead Sponsor: Ipsen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2009-09-15
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Greater than or equal to 18 years of age with idiopathic cervical dystonia. Toronto Western Spasmodic Torticollis Rating Scale score of greater than or equal to 15 and at least 12 weeks since last BoNT-A Injection.

Exclusion Criteria

Contraindication to BoNT-A
Secondary cervical dystonia

Study & Design

• Study Type: Observational
• Study Design: Not specified