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Comparative study for the effect of test diets on the absorption and excretion of the body water and electrolytes. -an open-label, randomized, two-periods crossover comparative trial

Not Applicable
Conditions
Heat stress disorder
Registration Number
JPRN-UMIN000052372
Lead Sponsor
IMEQRD Co., Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Male
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

1. Have been taking foods or supplements with functional health claims, which affect the study outcome, such as capsaicin, spices, or any stimulus functional foods for blood flow or body temperature improvement, more than three times a week, and who can't also discontinue intake of these foods. 2. Currently receive medical treatments with drugs. Medications used as needed are acceptable. 3. Alcohol drinking over an average of 40 g/day per week. 4. Have difficulty with blood sampling. 5. Those who have a tattoo. 6. Have difficulty with sweating in a sauna bath. 7. Those whose weight does not fluctuate due to sweating 8. Those who can't enter a sauna bath for ten minutes three times. 9. Those who can't enter a sauna bath for one person due to claustrophobia. 10. Have a scar for a burn injury in a wide area on the body. 11. Have severe diseases or a history of severe diseases in the heart, liver, kidney, or digestive organs. 12. Have allergies to drugs or foods. 13. Those who joined other clinical trials four weeks before, those who have currently joined other clinical trials, and who are planning to join other clinical trials after the consent acquisition in the study. 14. Have above 200 mL blood donation within one month before the start period of the study. 15. Have above 400 mL blood donation within three months before the start period of the study. 16. Have above 1200 mL blood donation volume, which is the sum of the planned blood donation volume in the study and the previous donated blood volume within twelve months before the start period of the study. 17. Those who are unsuitable for the study, judged by the principal investigator.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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