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Completed Phase 3 Interventional

A Clinical Research Study Testing Ropinirole Treatment for Restless Legs Syndrome

ClinicalTrials.gov ID: NCT00363857

Public ClinicalTrials.gov record NCT00363857. 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 Jun 26, 2026, 12:27 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 in Patients Suffering From Restless Legs Syndrome (RLS)

Study identification

NCT ID
NCT00363857
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
360 participants

Conditions and interventions

Interventions

  • Ropinirole Drug

Drug

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
Jul 31, 2003
Primary completion
Apr 30, 2004
Completion
Apr 30, 2004
Last update posted
Oct 16, 2016

2003 – 2004

United States locations

U.S. sites
49
U.S. states
25
U.S. cities
47
Facility City State ZIP Site status
GSK Investigational Site Alabaster Alabama 35007
GSK Investigational Site Birmingham Alabama 35294
GSK Investigational Site Jasper Alabama 35501
GSK Investigational Site Tuscaloosa Alabama 35406
GSK Investigational Site Phoenix Arizona 85032
GSK Investigational Site Phoenix Arizona 85050
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Berkeley California 94705
GSK Investigational Site La Jolla California 92037
GSK Investigational Site Northridge California 91325
GSK Investigational Site Oxnard California 93030
GSK Investigational Site Redondo Beach California 90277
GSK Investigational Site Santa Monica California 90404
GSK Investigational Site Stanford California 94305-5548
GSK Investigational Site Aurora Colorado 80012
GSK Investigational Site Danbury Connecticut 06810
GSK Investigational Site Boca Raton Florida 33486
GSK Investigational Site Largo Florida 33773
GSK Investigational Site Pembroke Pines Florida 33026
GSK Investigational Site St. Petersburg Florida 33701
GSK Investigational Site Tampa Florida 33606
GSK Investigational Site Tampa Florida 33609
GSK Investigational Site Atlanta Georgia 30329
GSK Investigational Site Augusta Georgia 30912
GSK Investigational Site Macon Georgia 31201
GSK Investigational Site Chicago Illinois 60611
GSK Investigational Site Elk Grove Village Illinois 60007
GSK Investigational Site Louisville Kentucky 40217
GSK Investigational Site Southfield Michigan 48034
GSK Investigational Site Henderson Nevada 89052
GSK Investigational Site Lebanon New Hampshire 03766
GSK Investigational Site Albuquerque New Mexico 87108
GSK Investigational Site Schenectady New York 12308
GSK Investigational Site Raleigh North Carolina 27607
GSK Investigational Site Columbus Ohio 43210-1296
GSK Investigational Site Concinnati Ohio 45219
GSK Investigational Site Dublin Ohio 43017
GSK Investigational Site Oklahoma City Oklahoma 73112
GSK Investigational Site Portland Oregon 97201
GSK Investigational Site Lafayette Hill Pennsylvania 19444
GSK Investigational Site Philadelphia Pennsylvania 19107
GSK Investigational Site Columbia South Carolina 29201
GSK Investigational Site Nashville Tennessee 37205
GSK Investigational Site Austin Texas 78756
GSK Investigational Site Dallas Texas 75231
GSK Investigational Site Plano Texas 75093
GSK Investigational Site Alexandria Virginia 22311
GSK Investigational Site Norfolk Virginia 23507
GSK Investigational Site Walla Walla Washington 99362

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00363857, 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 Oct 16, 2016 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00363857 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →