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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00478166
Other study ID # 2004-174
Secondary ID
Status Completed
Phase N/A
First received May 22, 2007
Last updated October 1, 2015
Start date July 2005
Est. completion date October 2007

Study information

Verified date April 2011
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardUnited States: Federal Government
Study type Observational

Clinical Trial Summary

The purpose of this study is to use fMRI techniques to explore a certain part of the brain associated with Alzheimer's disease known as the posterior cingulate. Determining the functionality of this brain region may help us diagnose AD more accurately, thus allowing earlier treatment.


Description:

The posterior cingulate is a key brain region suggested by recent studies to be affected in people at risk for Alzheimer's Disease (AD). Because the PC is affected very early in the course of AD and the region may have reduced function even prior to the onset of symptoms, further understanding of its functional role and its relationship to other brain regions may be helpful in detecting AD earlier and in monitoring disease progression and treatment. This project examines the role of the PC and its connections to other brain regions using functional magnetic resonance imaging (fMRI), a technique that allows us to examine the brain at work during tests of memory and decision-making. The main goal is to see if functional connections between brain regions are modulated by risk for AD.


Recruitment information / eligibility

Status Completed
Enrollment 206
Est. completion date October 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 55 Years to 65 Years
Eligibility Inclusion Criteria:

- Cognitively healthy

- (Controls Only) Parents survived past age 70 and did/do not have memory problems.

Exclusion Criteria:

- Claustrophobia

- Metallic or electronic implants

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Locations

Country Name City State
United States University of Wisconsin - Wisconsin Comprehensive Memory Program Madison Wisconsin

Sponsors (2)

Lead Sponsor Collaborator
University of Wisconsin, Madison VA Office of Research and Development

Country where clinical trial is conducted

United States, 

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