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Effect of hyper protect capsule on viability of probiotics that reach to the large intestines

Effect of hyper protect capsule on viability of probiotics that reach to the large intestines - Viability of probiotics that encapsulated in hyper protect capsule to the large intestines

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038798
Enrollment
12
Registered
2019-12-06
Start date
2019-12-06
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

N/A(healthy adults)

Interventions

Test food A
Take a hyper protect capsules which contain Bifidobacterium in a package. (Single ingestion) Test food B
Take a Bifidobacterium in a package. (Single ingestion)

Sponsors

Morishita Jintan Co., Ltd.
Lead Sponsor
Animal Function Science Laboratory, Department of Applied Biological Sciences, Faculty of Agriculture,Setsunan University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Healthy men and women of 20 years or older at the time of consent acquisition (2) The number of Bifidobacterium spp. (3) Person who the number of defecation per day is less than three times on average (4) Persons with stool characteristics (Bristol scale) 3 or 4 (5) BMI has a standard range (18.5-25) (6)A person who receives the explanation of the clinical trial in advance, understands the contents, agrees to the purpose, and obtains written consent from the person

Exclusion criteria

Exclusion criteria: (1) Those who underwent open surgery within half a year of the trial start (2) Those who have taken antibiotics for more than one week within half a year of the study start (3) Persons who are allergic to the test food (4) Those who plan to change their lifestyle significantly during the examination period (5) Persons who are chronically prone to diarrhea (meaning stools with mud or watery stools) (6) Patients with a history of significant liver dysfunction, renal dysfunction, or cardiovascular disease that is considered inappropriate for this study (7) A person suspected of having a chronic or acute infection (8) Those who are pregnant or nursing or who may be pregnant (9) Those who participated in other clinical trials within the past 1 month (10) Others who were judged by the study investigator to be inappropriate for this study

Design outcomes

Primary

MeasureTime frame
Evaluation of ingested viable probiotic bacteria that reached to colon. : The fecal number of viable bacteria ingested (Bifidobacterium)

Secondary

MeasureTime frame
Analysis on gut microbiota by 16S metagenomic analysis : Evaluation of the abundance of Bifidobacterium spp. in the feces

Countries

Japan

Contacts

Public ContactMamiko Kohno

Morishita Jintan Co., Ltd. Health Care Product Department

m_kohno@jintan.co.jp03-6206-8138

Outcome results

None listed

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