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Verification test of the effect of lactic acid bacterium containing foods intake on functions of the intestines.

Verification test of the effect of lactic acid bacterium containing foods intake on functions of the intestines. - Verification test of the effect of lactic acid bacterium containing foods intake on functions of the intestines.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000032411
Enrollment
30
Registered
2018-06-01
Start date
2018-06-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adult

Interventions

2-week intake of the test food Wash out 2-week intake of the placebo 2-week intake of the placebo Wash out 2-week intake of the test food

Sponsors

HUMA R&D CORP
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Age: 20 years or older, under 65 years of age 2)Gender: Japanese males and females 3)Persons who have had 3 to 5 bowel movements per week

Exclusion criteria

Exclusion criteria: 1)People who regularly drink or drink yogurt containing lactobacilli*Yogurt consumption will not be excluded if habit exists during the study. 2)Patients who cannot limit the use of drugs that may affect bowel movements (e.g., laxatives, intestinal regulators), health foods, specified health foods, functional labeling foods, health . 3)Subjects who were attending the hospital for bowel movements illness at study entry and were taking medications or taking over-the-counter laxatives. 4)Persons who are currently receiving treatment at a medical institution for gastrointestinal diseases that have an effect on the regulation of intestinal function, or those who have undergone. 5)Persons with or with a history of diseases that may significantly affect bowel movements, such as irritable bowel disease and ulcerative colitis. 6)Persons with or with a history of diseases such as diabetes, liver disease, kidney disease, or heart disease. 7)Persons currently undergoing exercise and diet therapy under the supervision of a physician. 8)Persons with diseases requiring constant medication. 9)Persons with a history of serious disease requiring medical treatment. 10)Persons with a history of drug or food allergy. 11)Subjects who are judged inappropriate as subjects based on the responses to the background questionnaire. 12)Subjects with significant deviations from reference ranges in pre-test physical, physical, and laboratory measurements. 13)Pregnant, lactating women, or women who wish to become pregnant during the study. 14)Persons with a current or past history of psychiatric disorders (e.g., depression). 15)Persons who work shift, such as night shift workers. 16)Patients who are receiving or have a history of drug dependence or drug abuse. 17)Individuals who have participated in other human clinical studies or are currently participating in other human clinical studies within the past 3 months. 18)Other subjects who are considered inappropriate as subjects by the investigator.

Design outcomes

Primary

MeasureTime frame
Intestinal flora , Defecation frequency, Fecal amount , Bristol Stool Form Scale

Secondary

MeasureTime frame
Vital signs

Countries

Japan

Contacts

Public ContactOchitani Daisuke

HUMA R&D CORP Clinical Development Division

ochitani@huma-c.co.jp81-3-3431-1260

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026