Study to Assess the Effectiveness of AboBoNT-A Injections for Adult Lower Limb Spasticity in a Real Life Cohort
NCT04050527 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 438
Last updated 2022-08-05
Summary
The purpose of the protocol is to assess the longitudinal attainment of person-centered and function related goals of patients who receive AbobotulinumtoxinA (aboBoNT-A) injections for adult lower limb spasticity over a period of 16 months.
Conditions
- Adult Lower Limb Spasticity
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Ipsen Medical Director · Ipsen
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-12-19
- Primary Completion
- 2022-07-29
- Completion
- 2022-07-29
Countries
- United States
- Australia
- Brazil
- Canada
- France
- Germany
- Italy
- Poland
- Russia
Study Locations
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