A post marketing, international, multicenter, observational, prospective, longitudinal study. The purpose of the study is to describe cervical dystonia sub-types with their injection protocols and response to BoNT-A.
Study Type
OBSERVATIONAL
Enrollment
404
Responder rate at peak effect following one BoNT-A injection cycle without any deviations from routine practice
Time frame: Around 4 weeks post injection
To describe TWSTRS change scores from inclusion (total score & subscales scores)
Time frame: Baseline, and around 4 weeks and 3 months post injection
To describe tremor change score from inclusion (TSUI scale)
Time frame: Baseline, and around 4 weeks and 3 months post injection
To describe the Cervical Dystonia Impact Profile (CDIP) 58 change from inclusion
Time frame: Baseline, and around 4 weeks post injection
To describe subject and investigator's CGI scores
Time frame: Around 4 weeks post injection
To identify prognostic factors for response (Exploratory Objective)
Time frame: baseline, and around 4 weeks and 3 months post injection
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Royal Prince Alfred Hospital
Camperdown, Australia
St Vincent's Hospital
Fitzroy, Australia
Austin Hospital
Heidelberg, Australia
Westmead Hospital
Penrith, Australia
Alfred Hospital
Prahran, Australia
AZ Sint Jan Brugge
Bruges, Belgium
UZ Gent
Ghent, Belgium
Unnamed facility
Leuven, Belgium
Centre Hospitalier de Liège, Domaine Universitaire Sart Tilmen
Liège, Belgium
AZ Sint Augustinus Wilrijk
Wilrijk, Belgium
...and 29 more locations