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GSK Ropinirole in Subjects with Restless Legs Syndrome 101468/191 Baseline (Form 2)

- 31-08-17 - 1 Formulier, 13 Itemgroepen, 59 Data-elementen, 1 Taal

Itemgroepen: General Information, Orthostatic Vital Signs, Baseline PLMI, Polysomnography, Baseline Inclusion Criteria, Baseline Exclusion Criteria, RLS rating scales, Vital signs, Concomitant Medication, Medical Procedures, Baseline Signs and Symptoms, Baseline Employment Status, Ramos Randomization and dispensing

Study ID: 101468/191 Clinical Study ID: SKF-101468/191 Study Title:A 12 Week, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of Ropinirole in Subjects with Restless Legs Syndrome (RLS) Suffering from Periodic Leg Movements of Sleep (PLMS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication: Restless Legs Syndrome

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GSK Ropinirole in Subjects with Restless Legs Syndrome 101468/191 Baseline (Form 2)

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GSK Ropinirole in Subjects with Restless Legs Syndrome 101468/191 Baseline (Form 2)

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