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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00737217
Other study ID # 2005-0464
Secondary ID
Status Completed
Phase N/A
First received August 15, 2008
Last updated June 24, 2013
Start date March 2006
Est. completion date April 2009

Study information

Verified date June 2013
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This research study will evaluate functions of memory, thinking, behavior, and daily life activities and how these relate to the measurement of certain chemicals (acetylcholine and dopamine) in the brain using an imaging procedure called positron emission tomography (PET). You may know that in Alzheimer's dementia (dementia is a disease where persons become forgetful and confused), a reduction in the amount of acetylcholine, a "neurotransmitter" substance (a chemical messenger that nerve cells need to communicate with each other), may be responsible for some of the memory and behavioral changes. At the present time, the investigators have no clear information on the levels of acetylcholine in the brain of patients with Parkinson's disease who also have memory or behavioral changes.


Recruitment information / eligibility

Status Completed
Enrollment 74
Est. completion date April 2009
Est. primary completion date April 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 50 Years to 85 Years
Eligibility Inclusion Criteria:

- PDD: Patients who meet the UK Parkinson's Disease Society Brain Bank Research Center (UKPDSBRC) clinical diagnostic criteria for PD with dementia (MMSE 18-25; n=28; age 50-85 years; M/F) are eligible for the study. Hoehn and Yahr stages I-III.

- PD. Patients with who meet the UKPDSBRC criteria for PD with a MMSE of >25 (n=28; age 50-85 years; M/F). Hoehn and Yahr stages I-III.

- Normal control subjects (n=16) (age 50-85 years; M/F).

- No current or past history of neurologic or psychiatric illness.

Exclusion Criteria:

- Any subjects on cholinergic, anti-cholinergic drugs will be excluded from the study.

- Current or past history of neurologic or psychiatric illness.

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Behavioral:
Behavioral assessment/questionnaire
Complete behavioral assessment/questionnaire

Locations

Country Name City State
United States University of Michigan Functional, Cognitive and Mobility Laboratory Ann Arbor Michigan

Sponsors (2)

Lead Sponsor Collaborator
University of Michigan Michael J. Fox Foundation for Parkinson's Research

Country where clinical trial is conducted

United States, 

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