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
NCT01239628 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 45
Last updated 2020-03-31
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
- Upper Limb Spasticity After Stroke
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Medical Director, Neurology · Ipsen
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-12-31
- Primary Completion
- 2015-12-31
- Completion
- 2015-12-31
Countries
- Belgium
Study Locations
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