ClinicalTrials.gov record
Terminated Phase 4 Interventional Results available

Carbidopa/Levodopa/Entacapone Versus Immediate Release (IR) Carbidopa/Levodopa on Non-motor Symptoms in Patients With Idiopathic Parkinson's Disease and Demonstrating Non-motor Symptoms of Wearing Off

ClinicalTrials.gov ID: NCT00642356

Public ClinicalTrials.gov record NCT00642356. 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 May 6, 2026, 12:50 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

An 8-week, Prospective, Randomized, Double-blind, Double-dummy, Active-controlled, Multi-center Comparison Study of the Effects of Carbidopa/Levodopa/Entacapone Versus Immediate Release Carbidopa/Levodopa on Non-motor Symptoms in Patients With Idiopathic Parkinson's Disease and Demonstrating Non-motor Symptoms of Wearing Off

Study identification

NCT ID
NCT00642356
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Novartis
Industry
Enrollment
14 participants

Conditions and interventions

Interventions

  • Carbidopa/levodopa/entacapone Drug
  • Immediate release carbidopa/levodopa Drug

Drug

Eligibility (public fields only)

Age range
30 Years to 85 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
Feb 29, 2008
Primary completion
Apr 30, 2009
Completion
Apr 30, 2009
Last update posted
Feb 17, 2011

2008 – 2009

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
20
Facility City State ZIP Site status
Xenoscience, Inc Phoenix Arizona 85004
South Coast Health Center Aliso Viejo California 92656
University of California Irvine California 92697
Coastal Neurological Medical Group, Inc La Jolla California 92037
Georgetown University Hospital Washington D.C. District of Columbia 20007
Sunrise Clinical Research, Inc Hollywood Florida 33021
Charlotte Neurological Services Port Charlotte Florida 33952
Cotton O'Neil Clinic Topeka Kansas 66606
University of Maryland School of Medicine Baltimore Maryland 21201
Neurology, Inc Columbia Missouri 65201
Dr. John's Mercy Medical Center St Louis Missouri 63141
Creighton U Medical Center, Dept of Neurology Omaha Nebraska 68131
Parkinson's Disease & Movement Disorders Commack New York 11725
Central New York Research Corporation Syracuse New York 13210
Neurological Care of Central NY Syracuse New York 13210
Duke University Durham North Carolina 27705
Neurology Associates Monroeville Pennsylvania 15146
University of Pittsburg Pittsburgh Pennsylvania 15213
University of Texas Southwestern Dallas Texas 75390
University of Texas Medical School Houston Texas 77030
Scott & White Hospital Temple Texas 76508

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 NCT00642356, 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 Feb 17, 2011 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00642356 live on ClinicalTrials.gov.

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