Viewing Study NCT00197080



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00197080
Status: COMPLETED
Last Update Posted: 2016-09-23
First Post: 2005-09-13

Brief Title: Ropinirole XR Extended Release In Patients With Restless Legs Syndrome
Sponsor: GlaxoSmithKline
Organization: GlaxoSmithKline

Study Overview

Official Title: A 12-Week Double-Blind Placebo Controlled Parallel Group Study to Assess the Efficacy and Safety of Ropinirole XR Extended Release in Patients With Restless Legs Syndrome
Status: COMPLETED
Status Verified Date: 2016-09
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: None
Brief Summary: The purpose of this study is to assess the efficacy and safety of ropinirole XR in the treatment of adults with Restless Legs Syndrome RLS
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