Viewing Study NCT00373542



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Study NCT ID: NCT00373542
Status: COMPLETED
Last Update Posted: 2016-10-28
First Post: 2006-09-07

Brief Title: 12-week Polysomnography Study of Ropinirole Controlled Release for Restless Legs Syndrome
Sponsor: GlaxoSmithKline
Organization: GlaxoSmithKline

Study Overview

Official Title: A 12-Week Multi-Center Double-Blind Placebo-Controlled Parallel Group Flexible Dose Polysomnography Study of Ropinirole Controlled Release for Restless Legs Syndrome RLS in RLS Patients With Sleep Disturbance and Periodic Limb Movements PLM During Sleep
Status: COMPLETED
Status Verified Date: 2016-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CR-RLS
Brief Summary: The purpose of this study is to assess the efficacy and safety of ropinirole CR-RLS in the treatment of patients with Restless Legs Syndrome and associated sleep disturbance and period limb movements during sleep
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None