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

Inclusion Criteria: * Subject able to comply with the protocol * Provision of written informed consent prior to collecting the data * Male or female patients of 18 years or older * Presenting with upper limb spasticity after stroke for which treatment with botulinum toxin A is indicated Exclusion Criteria: * The subject has already been included in this survey * Patients who already received BoNT-A treatment for upper limb spasticity * Patients with known intolerance for BoNT-A * Subjects unable to comply with the protocol