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临床试验/NL-OMON29030
NL-OMON29030招募中不适用

Glymphatic dysfunction in cognitive impairment: a memory clinic study

Maastricht University Medical Center0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
120

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

入选标准

  • Patients with mild Alzheimer's disease dementia, patients with mild cognitive impairment (MCI), and healthy subjects will be included.
  • In order to be eligible for the AD dementia-group, a subject must meet all of the following criteria:
  • - Mentally competent (MMSE=18) and able to give informed consent
  • - Informed consent before participation in the study
  • - Age > 55 years
  • - Diagnosis of dementia of the AD type
  • Criteria for the MCI-group:
  • - Mentally component (MMSE =18) and able to give informed consent
  • - Informed consent before participation in the study
  • - Age > 55 years
  • - Diagnosis of MCI or diagnosis of Mild Neurocognitive Disorder (DSM V)
  • Criteria for the control (cognitively normal) group:
  • - Mentally component (MMSE =18) and able to give informed consent
  • - Informed consent before participation in the study
  • - Age > 55 years
  • - MMSE = 26
  • - Average age and gender is similar to the patient groups

排除标准

  • A potential subject who meets any of the following criteria will be excluded from participation in this study:
  • - Any significant disease or unstable medical condition that could influence neuropsychological testing (with the exception of a MCI or AD diagnosis)
  • - Major depression (according to the DSM IV) (< 12 months ago)
  • - Psychiatric history (schizophrenia, schizoaffective disorder, bipolar disorder or any history of electroconvulsive therapy)
  • - Vascular dementia
  • - Ischemic or valvular heart disease or electrocardiographic evidence of atrial fibrillation
  • - Recent transient ischemic attacks and ischemic or haemorrhagic stroke or cerebrovascular accident (< 2 years or paired with cognitive decline within 3 months after incident)
  • - Obstructive sleep apnoea syndrome
  • - Normal Pressure Hydrocephalus, M. Huntington, Parkinson’s disease, Frontotemporal dementia, Motor neuron diseases, Multiple sclerosis, Epilepsy
  • - Systemic inflammation, such as active rheumatoid arthritis
  • - Diabetes
  • - Cognitive impairment due to alcohol/drug abuse
  • - Structural abnormalities of the brain, such as tumours or stroke lesions
  • - Inability to provide informed consent
  • - Any contraindication for MRI: metallic implants, pacemaker, claustrophobia, pregnancy, tattoos in the head/neck region
  • - Unwillingness to be informed about potential abnormal MRI-findings
  • Additional exclusion criteria for the control group:
  • - A known diagnosis of mild cognitive impairment, prodromal dementia or dementia
  • - Substantial memory complaints (according to participant)

研究者

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