跳至主要内容
临床试验/NCT01602198
NCT01602198终止不适用

24-week, Randomized, Double-blind, Placebo-controlled, Parallel Group Study of the Exelon® [Rivastigmine] Transdermal Patch in 120 APOE e4 Positive Amnestic MCI Patients

The Cleveland Clinic1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2011年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
1
试验地点
1
主要终点
Change in BOLD Response on Functional Magnetic Resonance Imaging (fMRI)

研究概览

简要总结

The goal of this project is to determine if task-activated fMRI is sensitive to the central cholinergic deficit associated with Mild Cognitive Impairment.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
55 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of amnestic MCI
  • In good general health with no diseases expected to interfere with the study
  • Ability to undergo MRI
  • Fluent in English
  • Stable prescription dosages 1 month prior to testing
  • Carrier of the APOE e4 allele (determined by blood draw at screening visit)

排除标准

  • Neurological illness/conditions
  • Medical illnesses/conditions that may affect brain function
  • Prior history of use of any cholinesterase inhibitor
  • Instable or severe cardiovascular disease or asthmatic condition

研究组 & 干预措施

Exelon transdermal patch

Active Comparator

Exelon [rivastigmine] transdermal patch

干预措施: Exelon [rivastigmine] transdermal patch (Drug)

Placebo transdermal patch

Placebo Comparator

Placebo transdermal patch

干预措施: Placebo transdermal patch (Drug)

结局指标

主要结局

Change in BOLD Response on Functional Magnetic Resonance Imaging (fMRI)

时间窗: baseline and 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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