Viewing Study NCT00355641



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Last Modification Date: 2024-10-26 @ 9:26 AM
Study NCT ID: NCT00355641
Status: COMPLETED
Last Update Posted: 2016-10-28
First Post: 2006-07-20

Brief Title: Long-Term Safety Of Ropinirole XR In Patients With Restless Legs Syndrome
Sponsor: GlaxoSmithKline
Organization: GlaxoSmithKline

Study Overview

Official Title: A 52-Week Open-Label Study to Assess the Long-Term Safety of Ropinirole Extended Release XR in Patients With Restless Legs Syndrome RLS
Status: COMPLETED
Status Verified Date: 2016-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The primary objective of this study is to assess the safety and tolerability of ropinirole XR in the long-term treatment up to 52 weeksof adults with 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