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Study of the Effects of Dopaminergic Medications on Dopamine Transporter Density in Subjects With Parkinson's Disease
This study has been completed.
Study NCT00129181   Information provided by Institute for Neurodegenerative Disorders
First Received: August 9, 2005   Last Updated: August 27, 2009   History of Changes

August 9, 2005
August 27, 2009
January 2005
December 2006   (final data collection date for primary outcome measure)
To determine the influence of short-term levodopa therapy on dopamine transporter density in early Parkinson's disease [ Time Frame: 1 year ] [ Designated as safety issue: No ]
- To determine the influence of short-term levodopa therapy on dopamine transporter density in early Parkinson’s disease.
Complete list of historical versions of study NCT00129181 on ClinicalTrials.gov Archive Site
  • To determine the influence of short-term treatment with cabergoline on dopamine transporter density in early Parkinson's disease [ Time Frame: 1 year ] [ Designated as safety issue: No ]
  • To further develop the AMADEUS consortium, a collaboration of clinical-imaging SPECT DAT sites able to obtain data using comparable techniques and transmit imaging to a central analysis site [ Time Frame: 2 years ] [ Designated as safety issue: No ]
  • - To determine the influence of short-term treatment with cabergoline on dopamine transporter density in early Parkinson’s disease.
  • - To further develop the AMADEUS consortium, a collaboration of clinical-imaging SPECT DAT sites able to obtain data using comparable techniques and transmit imaging to a central analysis site.
 
Study of the Effects of Dopaminergic Medications on Dopamine Transporter Density in Subjects With Parkinson's Disease
A Single-blinded Assessment of the Short-term Effects of Cabergoline vs. Carbidopa/Levodopa on SPECT Dopamine Transporter Density in Out-patient Subjects With Parkinson's Disease

This study investigates whether there is a change in 123iodine-2ß- carbomethoxy-3ß-(4-iodophenyl) tropane ([123I]ß-CIT) uptake after short-term treatment with levodopa compared to either dopamine agonist or placebo.

This is a multi-center, open-label study of short-term treatment with levodopa or cabergoline on striatal DATscan uptake in early Parkinson's disease. Approximately 120 Parkinson's disease subjects will be randomized to receive either carbidopa/levodopa, cabergoline or no treatment during a twelve week period. Subjects will undergo SPECT imaging with DATscan at screening and after 12 weeks. After twelve weeks carbidopa/levodopa and cabergoline treatment will be withdrawn and all subjects will undergo SPECT imaging with DATscan after 8 weeks (20 weeks after baseline).

 
Interventional
Diagnostic, Randomized, Single Blind (Investigator), Placebo Control, Parallel Assignment, Safety/Efficacy Study
  • Parkinson Disease
  • Parkinsonian Syndrome
  • Drug: cabergoline
  • Drug: carbidopa/levodopa
  • Procedure: DATscan and SPECT imaging
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
30
January 2007
December 2006   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • The subject is aged 40 years or older.
  • Written informed consent is obtained.
  • Subjects have a clinical diagnosis of idiopathic Parkinson's disease.
  • Hoehn and Yahr stages for subjects are I-II.

Exclusion Criteria:

  • The subject has atypical or drug-induced Parkinson's disease.
  • The subject has dementia.
  • The subject has clinically significant abnormal laboratory values, and/or clinically significant or unstable medical or psychiatric illness.
  • The subject is pregnant.
Both
40 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Austria,   Germany,   Italy,   Spain
 
NCT00129181
 
AMAD001
Institute for Neurodegenerative Disorders
  • Pfizer
  • GE Healthcare
Principal Investigator: Kenneth L Marek, MD The Institute for Neurodegenerative Disorders
Principal Investigator: John P Seibyl, MD The Institute for Neurodegenerative Disorders
Institute for Neurodegenerative Disorders
August 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP