Efficacy and Safety Study of Topiramate to Treat Restless Legs Syndrome
Restless Legs Syndrome
About this trial
This is an interventional educational/counseling/training trial for Restless Legs Syndrome focused on measuring Restless Legs Syndrome, Topiramate, Actigraphy, Polysomnography
Eligibility Criteria
Inclusion Criteria: The symptoms of each subject must meet the diagnostic criteria of the International RLS Study Group More than five periodic leg movements per hour recorded during baseline polysomnography (PSG) Each subject must discontinue all treatments for RLS and agreed not to take other RLS treatments during the study Exclusion Criteria: Clinically unstable medical problems History of nephrolithiasis Progressive neurologic disease Inadequate therapeutic response from two previous treatment regimens for RLS Subjects unable to discontinue medications known to cause or suppress RLS Subjects with sleep apnea syndrome Subjects consuming daily more than three beverages containing caffeine
Sites / Locations
- Neurocare