Healthy adult
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Subjects who have received sufficient explanation about the purpose and contents of this examination, have the ability to consent, fully volunteered with voluntary intention, agreed to participate in the document. (2) Subjects with an average of 4 or less bowel movements per week. (3) Subjects who have agreed to account registration for the smartphone app "Unlog", subjects who have already registered for an account.
Exclusion criteria
Exclusion criteria: (1) Subjects with chronic medical illness or a history of serious illness. (2) Subjects with underlying disease that causes chronic constipation, subjects with a history of gastrointestinal surgery. (3) Subjects who do not have a dietary habit of 3 meals a day. (4) Subjects with food allergies. (5) Subjects with lactose intolerance. (6) Subjects who took fermented milk such as yogurt, lactic acid bacteria drink, and natto at least 4 times a week during the month before the SCR test. (7) Subjects taking medications or quasi-drugs that may affect the study at least once a week, or subjects taking health foods at least four times a week, or subjects taking health foods four or more times a week during the month prior to the SCR test, or Subjects who plan to use these at least once during the study. (8) Subjects who have undergone gastroscopy, gastric X-ray barium, colonoscopy, colon cleansing or stool removal during the month prior to SCR, or during this study. (9) Subjects with or may have or have a history of IBS / organic constipation. (10) Subjects who participated in or plan to participate in other studies except observational studies during the month prior to the SCR test. (11) Women with changes in bowel movements during menstruation. (12) Pregnant subjects, subjects planning to become pregnant during the study period. (13) Breastfeeding subjects. (14) Smokers or subjects who quit smoking for less than 3 months. (15) Subjects who drink much alcohol. (16) Subjects who plan to move with night shifts or accommodation. (17) Subjects who are judged as ineligible by the clinical investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Compare the number of defecations in the week before ingestion with the number of defecations in the week from 1 week after ingestion to 2 weeks after ingestion. | — |
Secondary
| Measure | Time frame |
|---|---|
| Compare the stool properties for 1 week before ingestion with the stool properties for 1 week from 1 week after ingestion to 2 weeks after ingestion. | — |
Countries
Japan
Contacts
EP Mediate Co., Ltd. Development Business Headquarters, TTC Center, Trial Planning Department