KCT0004905尚未招募未知
A human study to evaluate the safety and effectiveness of HemoHIM on exercise performance and fatigue improvement
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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