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Functional Brain Imaging of Medication Treatment Response in Mild Alzheimer's Disease Patients

Phase 4
Terminated
Conditions
Alzheimer's Disease
Interventions
Registration Number
NCT00369603
Lead Sponsor
Duke University
Brief Summary

The purpose of this study is to determine whether standard medications approved for Alzheimer's disease treatment differ in their action on brain functioning and whether any observed brain activity differences as result of treatment are associated with particular patterns of dementia improvement or reduced decline.

Detailed Description

This study seeks to differentiate task-related and resting brain activity patterns captured via functional magnetic resonance imaging (fMRI) and associated with two common Alzheimer's disease (AD) medications, equivalent in acetylcholinesterase inhibition effect (AChEI) but differing with respect to allosteric nicotinic receptor modulation effect. It is the primary aim of this project to gain a better understanding of the brain mechanisms involved in the attentional and executive skills improvements associated with nicotinic receptor modulation in mild AD patients.

To address this question, this 12-week continuous treatment, double-blind, head-to-head dose-escalation treatment trial seeks to visualize any treatment response unique to allosteric nicotinic receptor modulation and to associate these fMRI data with standard cognitive assessment outcomes. Using in-scanner tasks shown to reliably elicit brain activity in cortical regions important to memory and attention, this treatment trial will examine both resting and task-related BOLD signal characteristics in a well-characterized sample of 36 mild AD patients after periods of low dose and high dose AD dementia treatment with either galantamine hydrobromide (AChEI + nicotinic receptor modulation) or donepezil hydrochloride (AChEI only). Both the low and high dose imaging comparisons between treatment groups will be equivalent for 35% AChEI-effect, which may allow for the isolation of BOLD signal unique to allosteric nicotinic receptor modulation in both brain at rest and task-related brain states.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
4
Inclusion Criteria
  • Must meet diagnosis of mild Alzheimer's disease
  • Must have a family member or caregiver who is willing to attend all study visits and provide information on your participation in the study
  • If female, must be post-menopausal
  • Must be able to swallow tablets
Exclusion Criteria
  • Metal implants or medical devises unsafe for MRI use
  • Pre-menopausal female
  • HIstory of recent head injury
  • Significant major, life-threatening illness or injury (e.g., stroke, AIDS, etc.)
  • Vascular dementia or any dementia other than Alzheimer's Disease
  • History of significant alcoholism or drug abuse
  • History of seizure disorder, developmental delay or major psychiatric illness

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Razadyne ERRazadyne ERgalantamine treatment group
AriceptAriceptAricept Treatment Group
Primary Outcome Measures
NameTimeMethod
Brain activity patterns, as collected via functional magnetic resonance imaging (fMRI), at rest and associated with task performance after 4 weeks of low-dose treatment and after 8-weeks of higher-dose treatment.4-weeks and 12-weeks
Secondary Outcome Measures
NameTimeMethod
Differences in cognitive testing and functional status at pre-treatment baseline and after completion of the 12-week treatment trial.baseline and 12-weeks

Trial Locations

Locations (1)

Joseph & Kathleen Bryan Alzheimer's Disease Research Unit

🇺🇸

Durham, North Carolina, United States

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