Trials / Terminated
TerminatedNCT01239628
A Prospective, Non-interventional Survey to Evaluate Injection Intervals and Treatment Modalities of Botulinum Toxin A (BoNT-A) in Adult Patients Suffering From Upper Limb Spasticity After Stroke
A National, Prospective, Non-interventional Survey to Evaluate Injection Intervals and Treatment Modalities up to 3 Years Follow up of Botulinum Toxin A in Adult Subjects Suffering From Upper Limb Spasticity Post-CVA (Cerebrovascular Accident)
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 45 (actual)
- Sponsor
- Ipsen · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the protocol is to evaluate injection intervals and treatment modalities up to 3 years follow-up of botulinum toxin A (BoNT-A) in adult patients suffering from upper limb spasticity after stroke.
Conditions
Timeline
- Start date
- 2010-12-01
- Primary completion
- 2015-12-01
- Completion
- 2015-12-01
- First posted
- 2010-11-11
- Last updated
- 2020-03-31
Locations
11 sites across 1 country: Belgium
Source: ClinicalTrials.gov record NCT01239628. Inclusion in this directory is not an endorsement.