Working… Menu
Trial record 64 of 332 for:    DONEPEZIL

Donepezil and Brain Activity Patterns in Those at Risk For Alzheimer's Disease

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00408525
Recruitment Status : Completed
First Posted : December 7, 2006
Last Update Posted : February 5, 2018
Information provided by (Responsible Party):
Vanderbilt University Medical Center ( Vanderbilt University )

Brief Summary:

The purpose of the study is to examine patterns of brain activity in people who are at risk for memory problems (e.g., Alzheimer's disease or dementia)before and after the medication donepezil. Although genetic testing will be done, the results will not be shared with study participants.

Once the genetic testing is completed subjects may continue to the second phase of the study. During this time they will be asked to take the medication donepezil (which is approved by the FDA for the treatment of Alzheimer's disease).

Donepezil is not FDA approved for healthy volunteers and is therefore considered investigational in this study.

Condition or disease Intervention/treatment Phase
Alzheimer's Disease Drug: donepezil Phase 1

Detailed Description:


  1. Cognitively intact individuals with normal brain morphology at genetic risk for developing Alzheimer's' Disease (AD) show alterations in brain activation patterns during tasks that require memory compared to similar individuals with lower risk for developing AD.
  2. Donepezil, a cholinesterase inhibitor, can normalize such brain activation patterns in subjects at risk for AD.


  1. To replicate a recent study1, and compare brain activation in subjects genetically at risk for AD (carriers of the є4 allele of the apolipoprotein E gene (APOE)) with subjects at lower risk for AD (lacking the є4 allele) during tasks that require memory, via functional magnetic resonance imaging (fMRI).
  2. To determine if administration of a drug currently indicated in the treatment of AD, donepezil, can reverse fMRI brain activation patterns of at risk subjects to patterns similar to those of subjects at lower genetic risk for AD.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 41 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: Efficacy of Donepezil in Normalizing Brain Activation Patterns in People Genetically at Risk for Alzheimer's Disease
Study Start Date : December 2006
Actual Primary Completion Date : August 24, 2012
Actual Study Completion Date : August 24, 2012

Arm Intervention/treatment
Experimental: 1
Drug: donepezil
donepezil 5 mg tablets, total dose per day 10 mg for 6 week duration of study. Taken once per day.
Other Name: Aricept

Primary Outcome Measures :
  1. Changes in brain activation patterns as measured in an fMRI. [ Time Frame: 8 weeks ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   40 Years to 85 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Subjects may report experiencing subjective memory dysfunction, however they must be found by clinical evaluation to have no memory dysfunction
  • Neuropsychological test battery in the normal range
  • Ages 40-85

Exclusion Criteria:

  • Dementia (Mini-Mental State Exam less than 25/30)
  • Left-handedness
  • Current medication that could influence cognition
  • Medical, psychiatric, and neurologic conditions, including cerebrovascular disease or uncontrolled hypertension
  • Claustrophobia
  • Surgical clips or implants
  • Pacemakers or other implanted electronic devices
  • History of sheet metal work

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 identifier (NCT number): NCT00408525

Layout table for location information
United States, Tennessee
Vanderbilt University Medical Center
Nashville, Tennessee, United States, 37212
Sponsors and Collaborators
Vanderbilt University
Layout table for investigator information
Principal Investigator: Harry E Gwirtsman, M.D. Vanderbilt University Medical Center


Layout table for additonal information
Responsible Party: Vanderbilt University Identifier: NCT00408525     History of Changes
Other Study ID Numbers: 040686
First Posted: December 7, 2006    Key Record Dates
Last Update Posted: February 5, 2018
Last Verified: February 2018
Keywords provided by Vanderbilt University Medical Center ( Vanderbilt University ):
memory loss
memory problems
Additional relevant MeSH terms:
Layout table for MeSH terms
Alzheimer Disease
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neurodegenerative Diseases
Neurocognitive Disorders
Mental Disorders
Cholinesterase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Cholinergic Agents
Neurotransmitter Agents
Physiological Effects of Drugs
Nootropic Agents