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Study ID

ROR104836

Study Title A parallel group study to evaluate the efficacy and safety of ropinirole for 26 weeks and to further evaluate the incidence of augmentation and rebound for a further 40 weeks open-label extension treatment period in subjects suffering from moderate to severe Restless Legs Syndrome.
Clinicaltrials.gov Identifier NCT00329602
Sponsor GlaxoSmithKline
Collaborators N/A
Study Recruitment Status Completed