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Study revised to use a different study medication and patient population.
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The goal of this project is to determine if task-activated fMRI is sensitive to the central cholinergic deficit associated with Mild Cognitive Impairment.
Clinical studies suggest that cholinesterase inhibitors (ChEIs) exert a cognitive benefit with chronic use among MCI and AD patients. Some studies also demonstrate a slight treatment benefit for persons who are APOE 4 positive. We propose to conduct a 24-week, randomized, double-blind, placebo-controlled, parallel group study of the Exelon® [rivastigmine] transdermal patch in 120 aMCI patients who have one or both APOE 4 alleles. Our preliminary analyses indicate that aMCI patients, even those who convert to AD, exhibit increased fMRI activation on our semantic memory activation task relative to not at-risk healthy participants and that increasing activation over time correlates with declines on neuropsychological testing. In addition, our preliminary data indicate that ChEI treated aMCI patients demonstrate normalization (i.e. reduction) in the magnitude of task-related neural activation over time relative to an untreated group. Furthermore, changes in fMRI magnitude demonstrated greater sensitivity to cholinergic modulation than changes on neuropsychological testing.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Exelon transdermal patch | Active Comparator | Exelon [rivastigmine] transdermal patch |
|
| Placebo transdermal patch | Placebo Comparator | Placebo transdermal patch |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Exelon [rivastigmine] transdermal patch | Drug | Exelon patch 1/day for six months |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in BOLD Response on Functional Magnetic Resonance Imaging (fMRI) | baseline and 6 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Stephen M Rao | The Cleveland Clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cleveland Clinic | Cleveland | Ohio | 44195 | United States |
No data to share.
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| ID | Title | Description |
|---|---|---|
| FG000 | Exelon Transdermal Patch | Exelon [rivastigmine] transdermal patch Exelon [rivastigmine] transdermal patch: Exelon patch 1/day for six months |
| FG001 | Placebo Transdermal Patch | Placebo transdermal patch Placebo patch: Placebo patch 1/day for 6 months |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Exelon Transdermal Patch | Exelon [rivastigmine] transdermal patch Exelon [rivastigmine] transdermal patch: Exelon patch 1/day for six months |
| BG001 | Placebo Transdermal Patch |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Change in BOLD Response on Functional Magnetic Resonance Imaging (fMRI) | Trial was terminated prematurely after enrollment of only 1 participant. Sample size is insufficient for BOLD response analysis. | Posted | baseline and 6 months |
|
Adverse events were collected during the study.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Exelon Transdermal Patch | Exelon [rivastigmine] transdermal patch Exelon [rivastigmine] transdermal patch: Exelon patch 1/day for six months |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| High blood pressure | Cardiac disorders | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Stephen Rao | Cleveland Clinic | 216-444-1025 | raos2@ccf.org |
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| ID | Term |
|---|---|
| D019965 | Neurocognitive Disorders |
| D060825 | Cognitive Dysfunction |
| ID | Term |
|---|---|
| D001523 | Mental Disorders |
| D003072 | Cognition Disorders |
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| ID | Term |
|---|---|
| D000068836 | Rivastigmine |
| D057968 | Transdermal Patch |
| ID | Term |
|---|---|
| D048448 | Phenylcarbamates |
| D002219 | Carbamates |
| D000144 | Acids, Acyclic |
| D002264 | Carboxylic Acids |
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| Placebo transdermal patch | Drug | Placebo transdermal patch 1/day for 6 months |
|
|
Placebo transdermal patch
Placebo patch: Placebo patch 1/day for 6 months
| BG002 | Total | Total of all reporting groups |
| Participants |
|
| Gender | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Units | Counts |
|---|
| Participants |
|
| 0 |
| 0 |
| 0 |
| 0 |
| EG001 | Placebo Transdermal Patch | Placebo transdermal patch Placebo patch: Placebo patch 1/day for 6 months | 0 | 1 | 1 | 1 |
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| D009930 |
| Organic Chemicals |
| D004864 | Equipment and Supplies |