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.
Full Title of Study: “Functional Neuroimaging (fMRI) Biomarker of Allosteric Nicotinic Receptor Modulation in Mild Alzheimer’s Disease Patients: A Razadyne vs. Aricept Dose Escalation Trial”
- Study Type: Interventional
- Study Design
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Primary Purpose: Treatment
- Masking: Triple (Participant, Care Provider, Investigator)
- Study Primary Completion Date: October 2007
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.
- Drug: Razadyne ER
- 4-weeks 8mg. Razadyne ER, then 4-weeks 16mg. Razadyne ER, and a subsequent 4-weeks of 24mg. Razadyne ER
- Drug: Aricept
- 8-weeks 5mg. Aricept and a subsequent 4-weeks of 10mg. Aricept
Arms, Groups and Cohorts
- Experimental: Razadyne ER
- galantamine treatment group
- Experimental: Aricept
- Aricept Treatment Group
Clinical Trial Outcome Measures
- 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.
- Time Frame: 4-weeks and 12-weeks
- Differences in cognitive testing and functional status at pre-treatment baseline and after completion of the 12-week treatment trial.
- Time Frame: baseline and 12-weeks
Participating in This Clinical Trial
- 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
Gender Eligibility: All
Minimum Age: 40 Years
Maximum Age: 90 Years
Are Healthy Volunteers Accepted: No
- Lead Sponsor
- Duke University
- Ortho-McNeil Neurologics, Inc.
- Provider of Information About this Clinical Study
- Overall Official(s)
- Jeffrey N Browndyke, PhD, Principal Investigator, Duke University
- Roberto Cabeza, PhD, Principal Investigator, Duke University
- James R Burke, PhD, Principal Investigator, Duke University
- Kathleen Welsh-Bohmer, PhD, Principal Investigator, Duke University
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