KCT0003766已完成未知
Evaluation of OFE on the Mild Cognitive Impairment for the Efficacy and Safety: A 12 week, Multi-center, Randomized, Double-blind, Placebo-controlled Clinical Trial
Koreaeundan0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 55(Year) 至 85(Year)（—）
- 性别
- All
入选标准
- •With subjective memory complaints
- •With Literacy
- •Who have scores in memroy domains of CERAD-K below -1.0 SD
- •Who agree informed consent
排除标准
- •Inpatient or within 3 months after discharge with malignancy, severe cerebrovascular diseasd, severe cardiac disease
- •Schizophrenia, major depressive disorder
- •Dementia, Parkinson disease, cerebral infarction
- •The patient who taking the cerebral enhancer test before 4 weeks
- •The patient who taking more than 400IU of vitamin E
- •Alcohol abuse or dependence
- •Thyroid disease
- •Renal or hepatic dysfunction
- •Uncontrolled high blood glucose and high blood preasure
- •Pregnancy or breast feeding
- •The patient who involved with 3 months with other human clinical trial
- •The patient who is not suitable for this clinical trial by investigator
研究者
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