A Multicentre, Interventional, Post-marketing, Randomised, Double-blind, Crossover Study to Evaluate the Clinical Safety and Efficacy of AbobotulinumtoxinA (Dysport) in Comparison With OnabotulinumtoxinA (Botox) When Treating Adults With Upper Limb Spasticity
Lay Description
Category
- IRB Number
- 20210554HU
- NCT Number
- ct.gov registration not required
- Open to Enrollment
- Yes
Eligibility
- Eligible Ages
- Eligible Genders
- Accepts Healthy Volunteers
Inclusion Criteria
Exclusion Criteria
Study Design
Arm Groups
Study Contact
Darcy Bair-Kelps
(210) 540-7100
bairkelps@uthscsa.edu
Monica Verduzco-Gutierrez
(210) 567-5350
gutierrezm19@uthscsa.edu
Hilda Pomroy
+1 (210) 450-9022
pomroy@uthscsa.edu
Monica Verduzco-Gutierrez
(210) 567-5350
gutierrezm19@uthscsa.edu
Hilda Pomroy
+1 (210) 450-9022
pomroy@uthscsa.edu
Principal Investigator
Monica Verduzco-Gutierrez