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Completed Phase 3 Interventional

Onset Motor Complications Using REQUIP CR (Ropinirole Controlled-release) As Add-on Therapy To L-dopa In Parkinson's

ClinicalTrials.gov ID: NCT00363727

Public ClinicalTrials.gov record NCT00363727. 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 26, 2026, 7:57 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 Two Year Phase IIIb Randomised, Multicenter, Double-blind, SINEMET Controlled, Parallel Group, Flexible Dose Study, to Assess the Effectiveness of Controlled Release Ropinirole add-on Therapy to L-dopa at Increasing the Time to Onset of Dyskinesia in Parkinson's Disease Subjects.

Brief summary

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

This study evaluates how effective a new formulation of a marketed drug is in increasing the time to onset of dyskinesia (abnormal twisting, writhing movements) in patients with Parkinson's Disease who have been taking levodopa for less than 2 years.

Study identification

NCT ID
NCT00363727
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
209 participants

Conditions and interventions

Eligibility (public fields only)

Age range
30 Years to 70 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
Dec 2003 (Type not available)
Primary completion
Jan 2006 (Actual)
Completion
Jan 2006 (Actual)
Last update posted
Jan 18, 2017

2003 – 2006

United States locations

U.S. sites
69
U.S. states
27
U.S. cities
64
Facility City State ZIP Site status
GSK Investigational Site Anniston Alabama 36207 —
GSK Investigational Site Birmingham Alabama 35216 —
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Phoenix Arizona 85006 —
GSK Investigational Site Sun City Arizona 85351 —
GSK Investigational Site Tucson Arizona 85712 —
GSK Investigational Site La Jolla California 92037 —
GSK Investigational Site Los Angeles California 90033 —
GSK Investigational Site Newport Beach California 92660 —
GSK Investigational Site Oxnard California 93030 —
GSK Investigational Site San Jose California 95126 —
GSK Investigational Site Walnut Creek California 94596 —
GSK Investigational Site Boulder Colorado 80304 —
GSK Investigational Site Danbury Connecticut 06810 —
GSK Investigational Site Newark Delaware 19713 —
GSK Investigational Site Boca Raton Florida 33486 —
GSK Investigational Site Fort Lauderdale Florida 33145 —
GSK Investigational Site Gainesville Florida 32611 —
GSK Investigational Site Miami Florida 33143 —
GSK Investigational Site Palm Beach Gardens Florida 33410 —
GSK Investigational Site Pembroke Pines Florida 33026 —
GSK Investigational Site Port Charlotte Florida 33952 —
GSK Investigational Site Tampa Florida 33606 —
GSK Investigational Site Tampa Florida 33612 —
GSK Investigational Site Augusta Georgia 30912 —
GSK Investigational Site Austell Georgia 30106 —
GSK Investigational Site Columbus Georgia 31901 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Boise Idaho 83702 —
GSK Investigational Site Chicago Illinois 60611 —
GSK Investigational Site Chicago Illinois 60637 —
GSK Investigational Site Hoffman Estates Illinois 60194 —
GSK Investigational Site Northbrook Illinois 60062 —
GSK Investigational Site Des Moines Iowa 50309-1426 —
GSK Investigational Site Kansas City Kansas 66160 —
GSK Investigational Site Elkridge Maryland 21075 —
GSK Investigational Site South Weymouth Massachusetts 2190 —
GSK Investigational Site West Yarmouth Massachusetts 02673 —
GSK Investigational Site Bingham Farms Michigan 48025 —
GSK Investigational Site Grand Rapids Michigan 49503 —
GSK Investigational Site Traverse City Michigan 49684 —
GSK Investigational Site Las Vegas Nevada 89109 —
GSK Investigational Site Edison New Jersey 08818 —
GSK Investigational Site Albany New York 12205 —
GSK Investigational Site Amherst New York 14226 —
GSK Investigational Site Rochester New York 14603 —
GSK Investigational Site Asheville North Carolina 28801 —
GSK Investigational Site Chapel Hill North Carolina 27516 —
GSK Investigational Site Raleigh North Carolina 27607 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Cincinnati Ohio 45267-0525 —
GSK Investigational Site Eugene Oregon 97401 —
GSK Investigational Site Medford Oregon 97504-8456 —
GSK Investigational Site Philadelphia Pennsylvania 19104 —
GSK Investigational Site Austin Texas 78756 —
GSK Investigational Site Dallas Texas 75231 —
GSK Investigational Site Dallas Texas 75235 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Houston Texas 77081 —
GSK Investigational Site Lubbock Texas 79410 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Alexandria Virginia 22311 —
GSK Investigational Site Richmond Virginia 23226 —
GSK Investigational Site Roanoke Virginia 24014 —
GSK Investigational Site Kirkland Washington 98034 —
GSK Investigational Site Seattle Washington 98101 —
GSK Investigational Site Tacoma Washington 98405 —
GSK Investigational Site Charleston West Virginia 25301 —
GSK Investigational Site Madison Wisconsin 53715 —

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 NCT00363727, 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 Jan 18, 2017 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00363727 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →