Healthy adults
Conditions
Interventions
Test food 1 (continuous ingestion) -Washout period(4weeks)-Test food 2 (continuous ingestion)
Test food 2 (continuous ingestion) -Washout period(4weeks)-Test food 1(continuous ingestion)
Sponsors
Suntory beverage & Food limited.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1)Male and Female subjects ranging in age from 20 to 50 at informed consent. (2)Subjects who feel swelling in their face and legs. (3)Subjects who can visit the designated facility on measurement days. (4)Subjects who can make self-judgment and voluntarily gave written informed consent.
Exclusion criteria
Exclusion criteria: (1)Subjects with a maximal blood pressure of less than 90 mmHg, or subjects with a maximal blood pressure of more than 130 mmHg. (2)Subjects in pregnancy or lactation (3)Subjects who donated their blood components and/or whole blood (0.2 L) within the past 4 weeks. (4)Males who donated their whole blood (0.4 L) within the past 12 weeks. (5)Females who donated their whole blood (0.4 L) within the past 16 weeks. (6)Males being collected in total of their blood (1.2 L) within the past 12 months and in this research. (7)Females being collected in total of their blood (0.8 L) within the past 12 months and in this research. (8)Subjects being under other clinical tests, or partook in those within the past four weeks, or will join those after the consent. (9)Subjects who meet any of the following: (a)suffering from heart, liver, or kidney disease (including complications of other diseases) (b)having a history of cardiovascular disease (c)diabetes (d)allergic to the test food and required one. (e)having a history of cancer or lymphedema (10)Subjects with dysphagia (11)Subjects who have a disease for which they are undergoing treatment and are taking pharmaceuticals (excluding applied drugs, OTC drugs, and quasi-drugs), or who are likely to take pharmaceuticals (excluding applied drugs, OTC drugs, and quasi-drugs) during the study period. (12)Subjects at risk ofc or other seasonal allergic symptoms during the study period. (13)Subjects who have periodically used OTC drugs, quasi-drugs and health-specific / functional / health foods including supplements, which might affect this study. (14)Females whose menstrual cycle is not stable. (15)Heavy alcohol drinkers or excessive smokers. (16)Subject who are scheduled to work day and night shifts and night shifts during this examination period. (17)Subjects who have difficulty maintaining daily routines (18)Others who were judged as inappropriate for participation by the principal investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Calf circumference | — |
Countries
Japan
Contacts
Public ContactShigeo Moriguchi
Suntory beverage & Food limited. Development & Designed Department
Outcome results
None listed