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临床试验/KCT0004905
KCT0004905尚未招募未知

A human study to evaluate the safety and effectiveness of HemoHIM on exercise performance and fatigue improvement

Seoul National University0 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
尚未招募
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
30(Year) 至 60(Year)(—)
性别
All

入选标准

  • Healthy adults men and women aged 30 to under 60 who complain of fatigue (28 or more on the fatigue scale)

排除标准

  • 1) Subject who is unable to perform cycle ergometer test
  • 2) Subject who constantly exercised (moderate or high-intensity) for 3 months prior to the first visit
  • 3) Those with a high level of cardiopulmonary endurance (maximum oxygen consumption of 1st and 2nd grade of 50% depending on age)
  • 4) Subject has a body mass index (BMI) of 18.5 kg / m2 or less or 30 kg / m2 or more
  • 5) Subject is over alcoholic
  • 6) Smoker and drug addict
  • 7) Insomnia
  • 8) Subject have any of the following (including past medical history) or are taking any related medicines: hyperlipidemia, asthma, musculoskeletal disorder and etc
  • 9) Subject who had a surgical operation 6 months prior to the first visit
  • 10) Subjects who consumed oriental medicine within 1 month prior to the first visit
  • 11) Subjects who consumed functional foods or related food to affect physical performance and fatigue (health supplements, fatigue recover supplements and so on)
  • 12) Subject with hypersensitivity to the test food or ingredients contained in the test food
  • 13) Subject who are pregnant or lactating women
  • 14) Subject in other clinical trials within one month of the first visit or plan to participate in other clinical trials during this human study period
  • 15) Subject unable to use smartphone
  • 16) Any condition that the principal investigator believes the subject is unsuitable for this study

研究者

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