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Research on the relationship between postprandial glycemic response and intestinal environment / lifestyle

Research on the relationship between postprandial glycemic response and intestinal environment / lifestyle - Research on the relationship between PPGR and intestinal environment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000042134
Enrollment
600
Registered
2020-10-18
Start date
2020-10-18
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

None listed

Sponsors

KSO Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Participants who are Males or Females aged 20 to 70 years at the time of screening test 2. Participants who are non-diabetic participants 3. Participants who have BMI values 18 to 30 4. Participants who have decision making skills and received sufficient study explanation. Participants who agree in writing to join the project independently after understanding the study explanation

Exclusion criteria

Exclusion criteria: 1. Participants who use antibiotics prior to or during study 2. Participants who are under diabetes or digestive disease treatments 3. Participants who use cardiac pacemaker device or implantable cardioverter defibrillator 4. Participants who have food allergy 5. Participants who cannot use cooking devices (e.g. microwave oven, can opener or kitchen scale) 6. Participants who are inevitable to hard exercise or manual labor during study period 7. Participants who will plan to have X-ray, CT scan or MRI taken during study period 8. Participants who will be in the water over 30 min per day during study period 9. Participants who have difficulty using mobile phones or sleep/activity measuring instrument 10. Participants who have a clinical history of drug dependence or alcoholic 11. Participants who enroll in an another clinical trial 12. Participants who are pregnancy, lactation, or planning to become pregnant 13. Participants who are judged as a unsuited for the study by principal investigator

Design outcomes

Primary

MeasureTime frame
Blood glucose level Gut microbiome

Secondary

MeasureTime frame
Oral microbiome Blood profile

Countries

Japan

Contacts

Public ContactEiji Yoshikawa

KSO Corporation Sales department

yoshikawa@kso.co.jp03-3452-7733

Outcome results

None listed

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