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Clinical Trial Summary

Spasticity is often observed as muscle tightness and stiffness in the upper and/or lower limbs. Upper limb spasticity can interfere with joint movement and its severity can range from mild to severe. This study will assess how effective OnabotulinumtoxinA is in treating pediatric participants with Spasticity. Change in disease activity will be evaluated. OnabotulinumtoxinA is approved drug for treatment of Spasticity. Approximately 106 pediatric participants aged 2-17 years with spasticity associated with cerebral palsy will be enrolled in approximately 10 sites across Mexico. Participants will receive OnabotulinumtoxinA as prescribed by their physician in accordance to local label and followed for 12 months. There is expected to be no additional burden for participants in this trial. Participants will attend regular visits to a hospital or clinic in their routine practice.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06150729
Study type Observational
Source AbbVie
Contact Angel Mario Coll Munoz
Phone +52 5543935017
Email angel.coll@abbvie.com
Status Recruiting
Phase
Start date September 8, 2023
Completion date May 31, 2025

See also
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