Spasticity Clinical Trial
Official title:
An Observational, Prospective, Multicentre, National Trial on the Benefit of Botulinum Toxin Type A (BoNT-A) Injections in Untreated Chronic Post-stroke Spastic Brazilian Patients
The purpose of this study is to document the effectiveness of treating chronic post-stroke spastic patients with Botulinum Toxin type A.
As this is a non-interventional study, the decision to prescribe the product must be taken
prior to, and independently from the decision to enrol the patient. This decision should be
made in accordance with routine clinical practice at the hospital concerned. The clinical
justification for prescribing any treatment should be recorded at the outset by the
prescribing clinician.
This study will not interfere with the routine practice of the investigator or with the
patient's treatment plan. Assessments will be done only if performed regularly in routine
practice.
This study will be conducted in Brazil, wherein Marketing Authorization has been granted for
the use of BoNT-A in the treatment of spasticity of the upper and lower limb in adult
post-stroke patients.
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