Verification of intestinal environment improvement by test food

Verification of intestinal environment improvement by test food - Verification of intestinal environment improvement by test food

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000055382

Enrollment

Registered

2025-09-01

Start date

2024-09-01

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

None listed

Interventions

Test food is taken for 4 weeks Placebo of control 1 is taken for 4 weeks

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1) Regular visitor of Matsuike Clinic 2) Women with mild constipation who are prescribed magnesium oxide whose age at the time of obtaining consent to participate in the study is 20 to 64 years old 3) Those who have received sufficient explanation about the purpose and content of this study, have the ability to consent, volunteered to participate voluntarily after understanding well, and can agree to participate in this study in writing 4) Those who can visit the hospital on the designated day and can receive an inquiry 5) Those who are deemed appropriate by the study investigator to participate in this study

Exclusion criteria

Exclusion criteria: 1) Persons with symptoms other than mild constipation 2) Persons who have no visit history for the past 3 months 3) Those who cannot be judged by the investigator without affecting the participation in the study 4) Persons with food allergies 5) Persons who habitually consume a food (regardless of manufacturer) that falls under the generic name of the test food. 6) Those who plan to become pregnant, breast-feeding, or possibly pregnant, and pregnant during the study period 8) Habitual smokers 7) Persons with alcoholism or other mental disorders 9) Persons who may change their lifestyle during the test period (night work, long trip, etc.) 10) Those who are planning to take health functional foods or supplement foods during the study period 11) Those who have been treated with hospitalization within the past 6 months 12) Persons currently participating in other human clinical trials, those who have not passed 3 months since participating in other human clinical trials 13) Other persons who are deemed inappropriate by the study investigator

Design outcomes

Primary

Measure	Time frame
alteration of intensional bacterial flora	—

Secondary

Measure	Time frame
Bowel movement Body weight	—

Countries

Japan

Contacts

Public ContactRyotaro Shiga

MORINAGA & CO., LTD. R & D Center

r-shiga-bb@morinaga.co.jp045-571-6140

Outcome results