The effect of the test diet on the absorption and excretion of water and electrolytes in the body under a heatstroke dehydration model
- Conditions
- Dehydration, heat stroke
- Registration Number
- JPRN-UMIN000053309
- Lead Sponsor
- GOSHU YAKUHIN CO., LTD.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- Male
- Target Recruitment
- 20
Not provided
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method