ACTRN12613000347763
已完成
未知
A randomised placebo-controlled clinical trial investigating the neurocognitive effects and in vivo mechanisms of action of Lacprodan(Registered Trademark) PL-20 in elderly participants with age-associated memory impairment.
概览
- 阶段
- 未知
- 干预措施
- 未指定
- 疾病 / 适应症
- Age-associated Memory Impairment (AAMI)
- 发起方
- Swinburne University of Technology
- 入组人数
- 138
- 状态
- 已完成
- 最后更新
- 6年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •Male or female.
- •\-Aged \>55 years.
- •\-Meets diagnostic criteria for age\-associated memory impairment: AAMI is defined on the basis of criteria first outlined by Crook et al: (i) A score \>25 on the Memory Complaint Questionnaire (MAC\-Q) and (ii) a score at \=1 standard deviation below the mean for healthy young adults on the Paired Associates Test from the Wechsler Memory Scale \- Revised (WMS\-R)
- •\-Willing and able to provide written informed consent.
- •\-Understands and is willing and able to comply with all study procedures.
- •\-English speaking.
- •\-Normal or corrected vision.
- •\-Must be right\-handed (applies only to the neuroimaging sub\-study).
排除标准
- •Dementia and/or MMSE score \<24\.
- •Neurological, cardiac, endocrine, gastrointestinal or bleeding disorders.
- •Psychiatric illness including mood disturbance/depression, as confirmed with a BDI\-II \>\=20\.
- •History of alcoholism and/or substance abuse.
- •Any known or suspected allergy to cow’s milk and/or lactose intolerance.
- •Participation in another clinical trial during the past 2 months.
- •Using any medications that could affect the outcome of the study including any pharmacological agents with known cognitive effects and diabetic medications.
- •Taking vitamins or herbal supplements regularly.
结局指标
主要结局
未指定
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