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Examination of the effects of Jerusalem artichoke inulin intake on gastrointestinal function and bowel movement improvement

Examination of the effects of Jerusalem artichoke inulin intake on gastrointestinal function and bowel movement improvement - Examination of the effects of Jerusalem artichoke inulin intake on gastrointestinal function and bowel movement improvement

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000042924
Enrollment
15
Registered
2021-01-12
Start date
2021-01-13
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 adults

Interventions

Dissolve 1 bag (high content) in drinks and take before breakfast daily. Dissolve 1 bag (low content) in drinks and take before breakfast daily. Dissolve 1 bag (placebo) in drinks and take before brea

Sponsors

IMEQRD Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 20 to under 64 at the time of informed consent 2. Japanese men and women 3. Subjects who deficate 2 to 5 times a week 4. Subjects who can input electronic diary with smartphone / PC 5. Subjects who understand the contents of the trial and obtain written consent before the trial based on the person's free will

Exclusion criteria

Exclusion criteria: Subjects who 1. are currently receiving any types of medicines and/or Chinese medical treatment (except for the drugs taken as needed). 2. are on a diet or exercise therapy under the supervision of a doctor. 3. have a current or history of serious illness. 4. are undergoing treatment for digestive disorders and constipation. 5. have had gastrointestinal surgery (appendicitis is acceptable). 6. take antiflatulent or laxatives daily. 7. take lactic acid bacteria drinks, yogurt or supplements containing lactic acid bacteria daily. 8. take foods for specified health use and foods with functional claims daily. 9. have a past and current medical history of drug or food allergy. 10. have participated in other clinical trials within one month before obtaining consent, or those who plan to participate during the trial period. 11. are currently pregnant or breastfeeding or those who want to become pregnant during the study period. 12. consume alcohol excessively (alcohol equivalent 60g or more / day). 13. have smoking habit. 14. have irregular life rhythms (work in shifts, work late at night etc.). 15. are judged by the investigator to be unsuitable for participating in this study.

Design outcomes

Primary

MeasureTime frame
Defecation survey (frequency of defecations)

Secondary

MeasureTime frame
Defecation survey (defecation volume, fecal properties by Bristol score and abdominal symptoms etc.), intestinal flora (by T-RFLP)

Countries

Japan

Contacts

Public ContactYoshitada Hira

IMEQRD Co., Ltd Planning and Sales Department

clinical-trial@imeqrd.co.jp03-6704-5968

Outcome results

None listed

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