跳至主要内容
临床试验/ISRCTN79036545
ISRCTN79036545已完成未知

Observational, correlational study aiming to identify healthy elderly subjects with Alzheimer pathology more efficiently

Centre for Human Drug Research0 个研究点目标入组 200 人开始时间: 2020年4月20日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
200

研究概览

简要总结

2021 Results article in https://pubmed.ncbi.nlm.nih.gov/34274005/ (added 19/07/2021) 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/35922871/ (added 04/08/2022)

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • 1. Aged 65 and older (inclusive)
  • 2. Willing and able to perform the cognitive tests, as evidenced by performance on the training session of the cognitive tests
  • 3. Willing and able to give written informed consent and to comply with the study procedures

排除标准

  • 1. Legal incapacity or inability to understand or comply with the requirements of the study
  • 2. Evidence of cognitive deterioration, as indicated by a diagnosis of a cognitive disorder (including but not limited to MCI, Alzheimer’s disease, Lewy Body Dementia, Fronto-temporal Dementia)
  • 3. History or symptoms of significant psychiatric disease in the past 3 years (including but not limited to clinical depression, schizophrenia);
  • 4. A Mini Mental State Examination (MMSE) score of =24
  • 5. A Geriatric Depression Scale – 15 (GDS) score of =6
  • 6. Presence of drug abuse, or positive urine drug screen (UDS) at screening or occasion
  • 7. Presence of severe alcohol abuse (daily alcohol consumption exceeding 2 standard drinks per day on average for females or exceeding 3 standard drinks per day on average for males (1 standard drink = 10 grams of alcohol)), or a positive breath alcohol test at screening or occasion
  • 8. Any contradictions for a lumbar puncture as judged by the principal investigator
  • 9. Any other reason that it is not safe or ethical to allow a subject to participate in the study in the opinion of the investigator

研究者

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