None listed
Conditions
Interventions
Subjects will take the functional food (high dose) once a day for 4 weeks.
Subjects will take the functional food (low dose) once a day for 4 weeks.
Subjects will take the placebo food once a day for
Sponsors
SUNTORY WELLNESS LIMITED
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1)Male and Female whose age are 20 <= years old <65. (2) Subjects who are troubled by their abdominal condition. (3) Subjects who can visit hospital on designated day. (4) Subjects who are able to submit the written informed consents.
Exclusion criteria
Exclusion criteria: (1) Subjects who are with treatment. (2) Subjects who constantly use drug medicine. (3) Subjects who are with history of gastrointestinal surgery. (4) Subjects who are attending other studies or attended other studies within the past 4 weeks. (5) Female in pregnancy, lactation and scheduled pregnancy period. (6) Subjects who are; a) With present heart disorder, liver disorder, kidney disorder or gastrointestinal tract disorder, b) With history of cardiac disorder or gastrointestinal tract disorder, c) With diabetes mellitus, or d) With allergy to the study foods. (7) Subjects who are not negative by virus immune serology test result at the time of screening. (8) Subjects who are deemed to be unsuitable by the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of subjects with improved abdominal conditions at the end of the trial compared to before intervention. | — |
Countries
Japan
Contacts
Public ContactKen-ichi Wakabayashi
SUNTORY WELLNESS LIMITED Institute for Health Care Science
Outcome results
None listed