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

Not Applicable
Conditions
/A(healthy adults)
Registration Number
JPRN-UMIN000038798
Lead Sponsor
Morishita Jintan Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
12
Inclusion Criteria

Not provided

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evaluation of ingested viable probiotic bacteria that reached to colon. : The fecal number of viable bacteria ingested (Bifidobacterium)
Secondary Outcome Measures
NameTimeMethod
Analysis on gut microbiota by 16S metagenomic analysis : Evaluation of the abundance of Bifidobacterium spp. in the feces
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