Viewing Study NCT00225862



Ignite Creation Date: 2024-05-05 @ 12:02 PM
Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00225862
Status: COMPLETED
Last Update Posted: 2016-09-15
First Post: 2005-06-30

Brief Title: A Clinical Research Study Evaluating Ropinirole Treatment For Restless Legs Syndrome RLS
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 Intermittent Dosing of Ropinirole in Patients With Restless Legs Syndrome RLS
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: A 12-week clinical research study to evaluate the tolerability efficacy and safety of ropinirole compared to placeboan inactive sugar pill in the treatment of patients with RLS in the United States
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