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Trial record 1 of 1 for:    NCT00139867
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A Multicenter, Open-label Trial to Assess Subject Preference of PARCOPA, Carbidopa/Levodopa Orally Disintegrating Tablets, Compared to Conventional Carbidopa/Levodopa Tablets in Subjects With Stable Parkinson's Disease

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ClinicalTrials.gov Identifier: NCT00139867
Recruitment Status : Completed
First Posted : August 31, 2005
Last Update Posted : October 20, 2014
Sponsor:
Information provided by:
UCB Pharma

Study Description
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Brief Summary:
The objective of this trial was to assess subject preference for PARCOPA, carbidopa/levodopa Orally Disintegrating Tablets (ODT), compared with conventional carbidopa/levodopa tablets, in subjects with stable Parkinson's disease.

Condition or disease Intervention/treatment Phase
Parkinson's Disease Drug: PARCOPA Phase 3

Detailed Description:
See approved Package Insert for Adverse Event information.
Study Design
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Study Type : Interventional  (Clinical Trial)
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Official Title: A Multicenter, Open-label Trial to Assess Subject Preference of PARCOPA, Carbidopa/Levodopa Orally Disintegrating Tablets, Compared to Conventional Carbidopa/Levodopa Tablets in Subjects With Stable Parkinson's Disease
Study Start Date : January 2004
Actual Primary Completion Date : May 2004
Actual Study Completion Date : May 2004

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Arms and Interventions
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Outcome Measures
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Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Criteria

Inclusion Criteria:

  • Stable Parkinson's Disease

Exclusion Criteria:

  • Not using carbidopa/levodopa tablets
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00139867


Locations
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United States, Wisconsin
Schwarz
Milwaukee, Wisconsin, United States
Sponsors and Collaborators
UCB Pharma
Investigators
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Study Director: UCB Clinical Trial Call Center UCB Pharma
More Information
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Additional Information:
Clinical Study Summary on UCB.com  This link exits the ClinicalTrials.gov site

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ClinicalTrials.gov Identifier: NCT00139867    
Other Study ID Numbers: SP0780
First Posted: August 31, 2005    Key Record Dates
Last Update Posted: October 20, 2014
Last Verified: September 2009
Additional relevant MeSH terms:
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Parkinson Disease
Parkinsonian Disorders
Basal Ganglia Diseases
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Movement Disorders
Neurodegenerative Diseases
Levodopa
Carbidopa
Carbidopa, levodopa drug combination
 Antiparkinson Agents
Anti-Dyskinesia Agents
Dopamine Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Aromatic Amino Acid Decarboxylase Inhibitors
Enzyme Inhibitors
Adjuvants, Immunologic
Immunologic Factors
Dopamine Agonists