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临床试验/KCT0004041
KCT0004041招募中未知

Depression realted to Bio-Cognitive-Neurophysiological Markers in AD, MCI, and geriatric depression

Hallym University Medical Center- Chuncheon0 个研究点目标入组 600 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
600

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
60(Year) 至 o Limit(—)
性别
All

入选标准

  • Inclusion Criteria
  • 1. Patients aged 60 years and older at the time of informed consent
  • 2. Patients who meet the following diagnosis criteria
  • 1) Diagnosis of Alzheimer’s disease and Mild cognitive disorder
  • - Patients who meet DSM-IV criteria and assessment via neuropsychological tests that used the Korean version of the Consortium to Establish a Registry for Alzheimer’s Disease Assessment Packet (CERAD-K)
  • 2). Diagnosis of depression
  • 1) AD patients who meet Olin’s diagnostic criteria for depression in AD
  • 2) MCI or elderly patients who meet DSM-IV and MINI-K
  • 3) Those who are able to decide voluntary participation in this clinical trial, agree in writing, and perform clinical procedures, including questionnaire preparation. However, if the patient is in a state where he or she can not make a voluntary decision due to a decline in cognitive function, a legal representative may decide to participate.

排除标准

  • Exclusion Criteria
  • 1) Patients who were taking any antidepressant medications within the previous 4 weeks
  • 2) Patients who show evidence of serious or unstable medical illnesses (eg, Heart failure, Angina pectoris, Myocardial infaction, Arteriosclerosis, diabetes mellitus, inflammatory disease, malignant tumor) or serious mental illness.
  • 3) Patients who have a history of brain cramps, brain surgery, natural brain disease, or temperamental affective disorder, and abnormal findings other than brain atrophy in brain fMRI
  • 4) Patients who have a history of hypersensitivity to the investigational drug
  • 5) Patients who have treated with memantine medication
  • 6) Patients who were participated in other clinical trials within 3 months
  • 7) Patients with AST (GOT) or ALT (GPT) > 2 times the upper normal limit or serum creatinine exceeding 150 umol /L(1.7 mg/dL)
  • 8) Patients who have a history of alcohol or other substance dependence
  • 9) Patients who have evidence of uncontrolled diabetes mellitus or hypertension
  • 10) Patients who is deemed inapropriated for the trial by investigator
  • 11) Patients who have serious serious dementia (GDS score ? 7 or CDR ? 4)

研究者

发起方
Hallym University Medical Center- Chuncheon

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