Trials / Completed
CompletedNCT01840462
Longitudinal Study for Treatment With Botulinum Toxin A Injections in naïve and Pre-treated Patients Suffering From Cervical Dystonia [CD-NIS-Longterm]
A National, Multicenter, Non-interventional, Prospective, Longitudinal Study for Treatment With Botulinum Toxin A Injections in naïve and Pre-treated Patients Suffering From Cervical Dystonia (Dysport®)
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 372 (actual)
- Sponsor
- Ipsen · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to investigate the efficacy of Dysport® in the treatment of cervical dystonia (CD) in a non-interventional long-term study in naïve and pre-treated patients.
Conditions
Timeline
- Start date
- 2012-07-01
- Primary completion
- 2015-11-01
- Completion
- 2016-03-01
- First posted
- 2013-04-25
- Last updated
- 2019-01-14
Locations
2 sites across 2 countries: Austria, Germany
Source: ClinicalTrials.gov record NCT01840462. Inclusion in this directory is not an endorsement.