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Completed Phase 4 Interventional

12-week Polysomnography Study of Ropinirole Controlled Release for Restless Legs Syndrome

ClinicalTrials.gov ID: NCT00373542

Public ClinicalTrials.gov record NCT00373542. 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 Jul 21, 2026, 9:58 AM 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, Multi-Center, Double-Blind, Placebo-Controlled, Parallel Group, Flexible Dose Polysomnography Study of Ropinirole Controlled Release for Restless Legs Syndrome (RLS) in RLS Patients With Sleep Disturbance and Periodic Limb Movements (PLM) During Sleep

Study identification

NCT ID
NCT00373542
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
39 participants

Conditions and interventions

Interventions

  • ropinirole CR-RLS 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
Sep 30, 2006
Primary completion
May 31, 2007
Completion
May 31, 2007
Last update posted
Oct 27, 2016

2006 – 2007

United States locations

U.S. sites
45
U.S. states
25
U.S. cities
44
Facility City State ZIP Site status
GSK Investigational Site Jasper Alabama 35501
GSK Investigational Site Tuscaloosa Alabama 35406
GSK Investigational Site Phoenix Arizona 85006
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Anaheim California 92801
GSK Investigational Site San Diego California 92108
GSK Investigational Site Greenwood Colorado 80111
GSK Investigational Site Wheat Ridge Colorado 80033
GSK Investigational Site Brandon Florida 33511
GSK Investigational Site Pembroke Pines Florida 33026
GSK Investigational Site St. Petersburg Florida 33707
GSK Investigational Site Atlanta Georgia 30342
GSK Investigational Site Austell Georgia 30106
GSK Investigational Site Macon Georgia 31201
GSK Investigational Site Elk Grove Village Illinois 60007
GSK Investigational Site Normal Illinois 61761
GSK Investigational Site Danville Indiana 46122
GSK Investigational Site Lenexa Kansas 66214
GSK Investigational Site Topeka Kansas 66606
GSK Investigational Site Crestview Hills Kentucky 41017
GSK Investigational Site Lexington Kentucky 40509
GSK Investigational Site Louisville Kentucky 40217
GSK Investigational Site Baton Rouge Louisiana 70808
GSK Investigational Site Lafayette Louisiana 70503
GSK Investigational Site Auburn Maine 04210
GSK Investigational Site Brighton Massachusetts 02135
GSK Investigational Site St Louis Missouri 63143
GSK Investigational Site Las Vegas Nevada 89104
GSK Investigational Site Toms River New Jersey 08755
GSK Investigational Site Charlotte North Carolina 28204
GSK Investigational Site Greenville North Carolina 27835
GSK Investigational Site Cincinnati Ohio 45246
GSK Investigational Site Cleveland Ohio 44195
GSK Investigational Site Dublin Ohio 43017
GSK Investigational Site Oklahoma City Oklahoma 73112
GSK Investigational Site Tulsa Oklahoma 74104
GSK Investigational Site Corvallis Oregon 97330
GSK Investigational Site Portland Oregon 97219
GSK Investigational Site Portland Oregon 97239
GSK Investigational Site Duncansville Pennsylvania 16635
GSK Investigational Site Lafayette Hill Pennsylvania 19444
GSK Investigational Site Columbia South Carolina 29201
GSK Investigational Site Dallas Texas 75213
GSK Investigational Site San Antonio Texas 78229
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 NCT00373542, 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 27, 2016 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00373542 live on ClinicalTrials.gov.

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