KCT0004042招募中未知
Effect of RP-1701 on the Mild Cognitive Impairment for the Efficacy and Safety; A 12week, Multi-center, Randomized, Double-blind, Placebo-Controlled Clinical Trial
Kyung Hee University Hospital0 个研究点目标入组 100 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
- 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
- •1) Adult men and women aged from 55 t0 85 years old who complain memory loss
- •2) Those who can decipher Korean
- •3) CERAD-K memory score decreased from 1.0SD to less than 2.0SD compare to the same age and education level gruop (CERAD word list memory or word delayed recall or word recognition)
- •4) A person who agrees to participate in the test and has signed an informed consent form
排除标准
- •1) A person who is admitted to hospital with malignant tumor, severe cerebrovascular disease (cerebral infarction, cerebral hemorrhage, etc.), severe heart disease (unstable angina, myocardial infarction, arrhythmia requiring heart failure treatment) or 3 months after discharge
- •2) A person with disease causing cognitive impairment such as dementia, Parkinson's disease,cerebral infarction etc.
- •3) A person who has experience of administering drugs (antipsychotic drugs, degenerative disease agents, brain function improvers, tricyclic antidepressants) for dementia or other cognitive dysfunction within 4 weeks
- •4) A person whose daily dose of vitamin E preparation is 400 IU or more, or whose dosage decreasing is inevitable.
- •5) A person who have received estrogen replacement therapy (excluding topical application agents) within 2 months of the start of the test
研究者
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