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临床试验/NCT00412048
NCT00412048撤回不适用

Evaluation of fMRI-SAM in the Early Detection of Alzheimer's Disease.

University Hospital, Strasbourg, France0 个研究点开始时间: 2012年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
主要终点
Comparing fMRI data between 3 groups of subjects: MCI, Alzheimer's disease and normal subjects

研究概览

简要总结

The aim of the protocol is to study the resting brain activation profile of 3 groups of people, using a new fMRI procedure, called fMRI-SAM. fMRI-SAM will be applied to 25 Alzheimer's disease (AD) patients, 25 patients suffering from amnestic - mild cognitive impairment (MCI) - a clinical picture which may be a prodromal form of AD - and 60 healthy controls. The first analysis of the data will search differences of brain activation profiles between the 3 groups. In the second step, the investigators will study the predictive value of fMRI-SAM to detect MCI patients who will later convert to AD.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
55 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Alzheimer's disease of mild to moderate severity (25 patients)
  • Amnestic MCI patients (25 patients)
  • 55-75 year-old patients

排除标准

  • Any other cause of dementia for AD patients
  • Any stroke
  • Any disease with a negative vital prognosis

研究组 & 干预措施

ALZHEIMER DISEASE

Other

干预措施: fMRI to detect MCI patients who will convert to Alzheimer's disease (Procedure)

MOLD COGNITIVE IMPAIRMENT

Other

干预措施: fMRI to detect MCI patients who will convert to Alzheimer's disease (Procedure)

CONTROLS

Other

干预措施: fMRI to detect MCI patients who will convert to Alzheimer's disease (Procedure)

结局指标

主要结局

Comparing fMRI data between 3 groups of subjects: MCI, Alzheimer's disease and normal subjects

时间窗: 1, 5 years

次要结局

  • Follow-up of MCI patients at 6, 12 and 18 months to detect a conversion to Alzheimer's disease(Prediction of Alzheimer's disease on fMRI data)

研究者

发起方
University Hospital, Strasbourg, France
申办方类型
Other
责任方
Sponsor

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