JPRN-UMIN000054058尚未招募Unknown
Verification of the effects of test food on cognitive function : Placebo-controlled, double-blind, randomized, two-phase, cross-over comparison study - Verification of the effects of test food on cognitive function : Placebo-controlled, double-blind, randomized, two-phase, cross-over comparison study
Miura Clinic, Medical Corporation Kanonkai0 个研究点目标入组 60 人开始时间: 2024年4月7日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 50years-old 至 79years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •(1) Subjects with Alzheimer's disease (2) Subjects with a history of stroke, subarachnoid hemorrhage, cerebral infarction, cerebral hemorrhage, cerebral contusion, or head injury (3) Subjects with a history of diabetes, liver diseases, renal disease, gastrointestinal disease, cardiac disease, respiratory disease, peripheral vascular disease, or other serious disease. (4) Subjects who have undergone gastrointestinal surgery (5) Subjects with abnormal liver and renal function test value (6) Subjects with diseases currently being treated (7) Subjects who are allergic to food and drugs (8) Subjects with anemia symptoms (9) Subjects with color discrimination difficulties (10) Subjects who have difficulty performing cognitive function tests due to low visual acuity, or who have been diagnosed with low vision or blindness (11) Subjects who have depression or have been diagnosed with depression (12) Subjects with motor, visual or hearing impairments (13) Subjects who play intense sports and subjects who are on a diet (14) Subjects who work at night or have other irregularities in their daily life during the examination period (15) Subjects who cannot stop taking health foods (including foods for specified health use and foods with functional claims) and quasi-drugs during the test period (16) Subjects who are continuously treated with pharmaceuticals (including OTC and prescription drugs) (17) Subjects who drink more than 20 g of average daily pure alcohol (18) Subjects who are participating in or will participate in other clinical trials at the start of this study. (19) Other subjects judged by the investigator or the investigator to be inappropriate for the examination
研究者
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