JPRN-UMIN000053309已完成Unknown
The effect of the test diet on the absorption and excretion of water and electrolytes in the body in a heatstroke dehydration model - A randomized, double-blind, placebo-controlled, two-periods cross-over comparative trial - - The effect of the test diet on the absorption and excretion of water and electrolytes in the body in a heatstroke dehydration model - A placebo-controlled, double-blind, cross-over trial
GOSHU YAKUHIN CO., LTD.0 个研究点目标入组 20 人开始时间: 2024年1月15日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 20
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
- 20years-old 至 ot applicable（—）
- 性别
- Male
入选标准
- 未提供
排除标准
- •1. Those who regularly use foods or supplements with functional health claims that may affect the study outcome three times or more a week and cannot stop them from the time of consent acquisition (e.g., health foods containing capsaicin, spices, or other strong stimulants that have effects such as improving blood flow, increasing body temperature, or inducing sweating). 2. Currently receiving drug therapy (however as-needed medication is acceptable.) . 3. Heavy alcohol drinker with a habit of drinking over an average of 40 g/day per week. 4. Those who have difficulty with blood sampling. 5. Those who have a tattoo. 6. Those who feel difficulty with sweating in a sauna bath. 7. Subjects without body weight fluctuation due to sweating. 8. Those who can't enter a sauna bath for ten minutes three times. 9. Those who can't enter an one person sauna bath due to claustrophobia. 10. Those who have a scar for a burn injury in a wide area on the body. 11. Those who have severe diseases or a history of severe diseases in the heart, liver, kidney, or digestive organs. 12. Those who have allergies to drugs or foods. 13. Those who are participating in clinical studies of other drugs or health foods, within 4 weeks after the end of the study, or who plan to participate in other clinical studies after consenting to participate in the study. 14. Those who donated blood components or whole blood of 200 mL within one month before the start of the study. 15. Those who have blood donation above 400 mL within three months before the start of the study. 16. Those whose total blood collection volume, including the planned volume for the study and the volume collected in the previous 12 months, exceeds 1200 mL prior to the initiation of the study. 17. Those who are deemed unsuitable for participation in the study by the principal investigator or the sub-investigator.
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