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Completed Phase 3 Interventional

Ropinirole XR (Extended Release) In Patients With Restless Legs Syndrome

ClinicalTrials.gov ID: NCT00197080

Public ClinicalTrials.gov record NCT00197080. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 4:52 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT00197080
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
380 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 79 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2005 (Type not available)
Primary completion
Not listed
Completion
Jan 2006 (Actual)
Last update posted
Sep 23, 2016

2005 – 2006

United States locations

U.S. sites
60
U.S. states
26
U.S. cities
58
Facility City State ZIP Site status
GSK Investigational Site Alabaster Alabama 35007 —
GSK Investigational Site Jasper Alabama 35501 —
GSK Investigational Site Mesa Arizona 85201 —
GSK Investigational Site Peoria Arizona 85381 - 4828 —
GSK Investigational Site Phoenix Arizona 85032 —
GSK Investigational Site Sun City Arizona 85351 —
GSK Investigational Site Anaheim California 92801 —
GSK Investigational Site Northridge California 91325 —
GSK Investigational Site Oxnard California 93030 —
GSK Investigational Site Pasadena California 91105 —
GSK Investigational Site Redondo Beach California 90277 —
GSK Investigational Site San Diego California 92103 —
GSK Investigational Site Santa Monica California 90404 —
GSK Investigational Site Colorado Springs Colorado 80909 —
GSK Investigational Site Denver Colorado 80212 —
GSK Investigational Site Wheat Ridge Colorado 80033 —
GSK Investigational Site Largo Florida 33773 —
GSK Investigational Site Pembroke Pines Florida 33026 —
GSK Investigational Site Stuart Florida 34996 —
GSK Investigational Site Atlanta Georgia 30338 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Austell Georgia 30106 —
GSK Investigational Site Dawsonville Georgia 30534 —
GSK Investigational Site Macon Georgia 31201 —
GSK Investigational Site Woodstock Georgia 30189 —
GSK Investigational Site Northbrook Illinois 60062 —
GSK Investigational Site Lenexa Kansas 66214 —
GSK Investigational Site Topeka Kansas 66606 —
GSK Investigational Site Louisville Kentucky 40217 —
GSK Investigational Site Baton Rouge Louisiana 70808 —
GSK Investigational Site Newton Massachusetts 02459 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Las Vegas Nevada 89119 —
GSK Investigational Site Albuquerque New Mexico 87108 —
GSK Investigational Site Albany New York 12205 —
GSK Investigational Site Endwell New York 13760 —
GSK Investigational Site Kingston New York 12401 —
GSK Investigational Site Schenectady New York 12308 —
GSK Investigational Site Raleigh North Carolina 27607 —
GSK Investigational Site Cincinnati Ohio 45236 —
GSK Investigational Site Cleveland Ohio 44130 —
GSK Investigational Site Dublin Ohio 43017 —
GSK Investigational Site Westerville Ohio 43081 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Portland Oregon 97219 —
GSK Investigational Site Lafayette Hill Pennsylvania 19444 —
GSK Investigational Site Columbia South Carolina 29201 —
GSK Investigational Site Mt. Pleasant South Carolina 29464 —
GSK Investigational Site Jackson Tennessee 38305 —
GSK Investigational Site Dallas Texas 75231 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Salt Lake City Utah 84102 —
GSK Investigational Site Salt Lake City Utah 84121 —
GSK Investigational Site Alexandria Virginia 22311 —
GSK Investigational Site Charlottesville Virginia 22911 —
GSK Investigational Site Bellingham Washington 98226 —
GSK Investigational Site Renton Washington 98055 —
GSK Investigational Site Spokane Washington 99204 —
GSK Investigational Site Walla Walla Washington 99362 —
GSK Investigational Site Wenatchee Washington 98801 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00197080, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 23, 2016 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00197080 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →