Observational Study With Neupro® to Evaluate the Patient´s Perception of Pain Associated With Parkinson´s Disease

Inclusion Criteria

• •The decision by the treating physician to treat a patient with Neupro® for the first time is made before the patient's participation in this Non-Interventional Study (NIS)
• •A Patient Data Consent form is signed and dated by the patient
• •Male and female patients that suffer from pain associated with idiopathic Parkinson's Disease according to the physician's assessment
• •Patients have not been treated with Rotigotine in the past