None listed
Conditions
Interventions
None listed
Sponsors
Suntory Global Innovation Center Ltd.
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: (1) Males who are 20 <= years old <40. (2) Subject who can come to the facility on the designated day. (3) Subjects who can make self-judgment and are voluntarily giving written informed consent.
Exclusion criteria
Exclusion criteria: (1) Subjects whose systolic pressure <90 mmHg. (2) Subjects who donated over 200ml whole blood within 4 weeks. (3) Subjects who donated over 400ml whole blood within 12 weeks. (4) Subjects whose blood was collected more than 1200 mL within the last 12 months when the amount of blood sampling in the current study is added. (5) Subjects who are participating in other clinical studies, or who finished clinical study within 4 weeks. (6) Subjects who are applicable to following items a) Subjects with disease on heart, liver, kidney or other organs complication. b) Subjects with a previous history of disease on circulatory organs. c) The subjects who are contracting diabetes. (7) Subjects who have severe allergic rhinitis. (8) Subjects who are on a diet or have a plan. (9) Subjects who have an unsteady lifestyle because of a working shift or a night shift. (10) Subjects who drink a lot. (11) Smoker (12) Subjects whose BMI is less the 18.5 or over 30.0. (13) Subjects whose systolic pressure >160 mmHg or diastolic pressure >100 mmHg. (14) Subjects who are judged as unsuitable for the study by the result of clinical examination and physical examination. (15) Subjects who are judged as unsuitable for the study by the principal investigator for other reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Amount of brown adipose tissue | — |
Secondary
| Measure | Time frame |
|---|---|
| Total energy expenditure | — |
Countries
Japan
Contacts
Public ContactAkiko Tateishi
Suntory Global Innovation Center Ltd. Research Institute
Outcome results
None listed