跳至主要内容
临床试验/NL-OMON43551
NL-OMON43551撤回不适用

Cross-sectional characterisation of elderly using the NeuroCart. - Cross-sectional NeuroCart study in elderly.

Centre for Human Drug Research0 个研究点目标入组 1,000 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
入组人数
1,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Males and females, aged 60 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 severe cognitive deterioration, as indicated by a diagnosis of severe cognitive disorder (including but not limited to Alzheimer*s disease, Lewy Body Dementia, Fronto-temporal Dementia);
  • 3. History or symptoms of significant psychiatric disease (including but not limited to clinical depression, schizophrenia);
  • 4. A Mini Mental State Examination (MMSE) score of < 18;
  • 5. A Geriatric Depression Scale (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 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

相似试验