跳至主要内容
临床试验/KCT0009298
KCT0009298招募中Unknown

A 12-week, Randomized, Double-blind, Placebo-controlled Multi-center Study to Investigate the Efficacy and Safety of CKDB001 on Cognitive-enhancing Function

Chong Kun Dang Bio0 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
Unknown
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

入排标准

年龄范围
55(Year) 至 80(Year)(—)
性别
All

入选标准

  • 1) Individuals who have voluntarily given written informed consent after receiving sufficient explanation about this human application trial.
  • 2) Adult men and women aged 55 to less than 80 years as of the date of written consent.
  • 3) Individuals who are capable of understanding Korean.
  • 4) Individuals whose score on the SVLT-E of the SNSB-II is decreased by more than 1.0 SD but less than 2.0 SD compared to the normal standard for the same education level and age group.

排除标准

  • - Individuals with any of the following medical histories or surgical/procedural histories: diseases accompanied by cognitive impairment, history of mental illness that may affect this human application trial, history of infections affecting brain function, severe concomitant diseases/disabilities deemed unsuitable for study participation by the researcher, etc.
  • - Individuals who have taken the following drugs and food within 4 weeks of Visit 2 (Baseline): those who have been administered or are expected to be administered during the study period drugs that can affect cognitive function, those who have continuously consumed or are expected to consume health functional foods or dietary supplements related to cognitive and memory improvement, etc.
  • - Individuals with hypersensitivity to any component of the test food or other allergies deemed unsuitable for study participation by the researcher's opinion.
  • - Pregnant or breastfeeding women.
  • - Women of childbearing potential and men who are unwilling or unable to use appropriate contraception methods during the study period.
  • - Individuals who have participated in another study involving clinical trial drugs, foods, or medical devices within the past 3 months.
  • - Any other reasons deemed by the researcher as inappropriate for conducting the study.

研究者

发起方
Chong Kun Dang Bio

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