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临床试验/NCT02377206
NCT02377206已完成早期 1 期

Neuroinflammation and Cognitive Decline in Alzheimer Disease (AD) : Pilot Study of Translocator Proteins Ligand PET Imaging With [18F]DPA-714

University Hospital, Tours6 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2016年4月6日最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
24
试验地点
6
主要终点
Compare the neuroinflammation measured by fixing and layout of [18F]DPA-714 between 3 groups of patients : subjects suffering from Alzheimer disease light to mild stage, amnesiac MCI and patients suffering from isolated cognitive complaint

研究概览

简要总结

The purpose of this study is to assess the level of neuroinflammation in Alzheimer Disease subject (mild to moderate) estimated with Binding Potential (BP) of [18F]DPA-714, and its relationship with the kinetics of cognitive decline over a 24-month follow-up period (as assessed by Alzheimer's Disease Assessment Scale-cognitive subscale (ADAS-Cog) and Mini-Mental State Examination (MMSE) scores).

详细描述

The purpose of this study is to assess the level of neuroinflammation in Alzheimer Disease subject (mild to moderate) estimated with Binding Potential (BP) of [18F]DPA-714 , and its relationship with the kinetics of cognitive decline over a 24-month follow-up period (as assessed by ADAS-Cog and MMSE scores).

(DPA-714 : N,N-diethyl-2-[4-(2-fluoroethoxy)phenyl]-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-acetamide)

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Informed consent
  • Age more than 50 years (included)
  • necessary knowledge of French (write and oral) to do neuropsychological tests
  • Study level upper (or equal) than 7 years (considering first year of grammar-school as start)
  • People with Alzheimer Disease defined as National Institute of Neurological and Communicative Disorders and Stroke (NINCDS) and the Alzheimer's Disease and Related Disorders Association (ADRDA) standards : Light to mild AD defined by Mini-Mental State Examination (MMSE) score between 15 and 25 (included)
  • Social security affiliation.

排除标准

  • MMSE score lower than 15 and upper or equal to 26
  • Evolutive disease which could possibly had consequences on central nervous system
  • Inflammatory disease or evolutive neoplasia and/or C reactive protein (CRP) upper than 10mg/L
  • Chronic use of alchohol and/or drug
  • Serious depression defined by Montgomery Asberg Depression Rating Scale (MADRS) score higher than 18
  • Surgical or medical condition in the last 3 months
  • Long term treatment which could possibly interfere with inflammatory process (especially the month before PET [18F]DPA-714 imaging).
  • Treatment by N-Methyl-D-Aspartate antagonist
  • Treatment by Minocycline
  • Treatment by benzodiazepine (especially the month before PET [18F]DPA-714 imaging) (Zolpidem, zopiclone and loprazolam excepted)
  • Anomaly at neurological examination which is not a classical symptom
  • Contraindication to magnetic resonance imaging (RMI)
  • Florbetapir[18F] hypersensibility
  • Participation to an other experimental protocol with drug.
  • people under guardianship

结局指标

主要结局

Compare the neuroinflammation measured by fixing and layout of [18F]DPA-714 between 3 groups of patients : subjects suffering from Alzheimer disease light to mild stage, amnesiac MCI and patients suffering from isolated cognitive complaint

时间窗: inclusion and 24 months

次要结局

  • Relationship passessment between [18F]DPA-714 fixing(Inclusion and 34 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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