None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Male healthy subjects aged 20 years or older at the time of consent (2) Subjects who can visit the designated medical institution on the scheduled visit date (3) Subjects who can enter an electronic diary using a PC, smartphone, etc. (4) Subjects who have been fully explained the purpose and content of the study, fully understood it, voluntarily volunteered to participate, and provided written consent to participate in the study.
Exclusion criteria
Exclusion criteria: Representative items are listed below. (1) Subjects with a systolic blood pressure of less than 90 mmHg (2) Subjects who have donated blood components or collected 200 mL or more of whole blood from 4 weeks before the start of the study until the start of the study (3) Subjects who have collected 400 mL or more of whole blood from 12 weeks before the start of the study until the start of the study (4) Subjects whose total planned blood collection for the study exceeds 1200 mL when added to the amount of blood collected from the month 12 months before the start of the study (5) Subjects who are participating as test subjects in other studies or who have completed a study within 4 weeks of participating*1 (6) Subjects who meet any of the following criteria a) Subjects with heart, liver, or kidney disease (including complications of other diseases) b) Subjects with a history of cardiovascular disease c) Subjects with diabetes*2 d) Subjects with allergies to the test foods*3 e) Subjects with a history of serious diseases such as cancer or tuberculosis (7) Subjects who are undergoing treatment at the time of screening (8) Subjects who regularly*4 take health foods or supplements such as foods for specified health uses or functional foods that may affect the study and cannot stop taking them from the time of consent (9) Subjects who smoke*5 (10) Subjects who consume more than 40 g of alcohol per day*6 (11) Subjects with extremely irregular eating habits (12) Shift workers or night workers (13) Subjects who have difficulty obtaining blood samples (14) Subjects who weigh less than 50 kg (15) Subjects who are obese (BMI 25 and above)*7 (16) Subjects who are otherwise deemed inappropriate for the study by the principal investigator or sub-investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Weight change | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Physiological test: body temperature, blood pressure, pulse rate 2. Blood biochemistry test: total protein (TP), albumin (Alb), Na, K, Cl, creatinine (CRE), glucose (GLU), osmolality 3. Urine test: excretion amount, Na, K, Cl, CRE, osmolality 4. FENa value (urinary sodium) 5. Electrolyte balance and water balance 6. Core body temperature 7. Oral water value at rest 8. Physical symptoms (questionnaire) | — |
Countries
Japan
Contacts
Suntory beverage & Food limited. Development & Designed Department