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A study using intermittently scanned continuous glucose monitoring of second meal effect of food containing some nutrients having suppressive effect on postprandial blood glucose level

A study using isCGM of second meal effect of food containing some nutrients having suppressive effect on postprandial blood glucose level - A study of second meal effect of food containing some nutrients having suppressive effect on postprandial blood glucose level

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000049000
Enrollment
100
Registered
2022-09-22
Start date
2022-09-22
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

1. Packed rice : During the 14-day test period, the number of intakes is 2 times for breakfast and 4 times for lunch, a total of 6 times 2. Test food : During the 14-day test period, the number of

Sponsors

LaViena Inc.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Males and females (>=20 to <=69 years of age) (2) Subjects whose BMI values are <=30 kg/m2 (3) Subjects who have and can use smartphone (iPhone : iOS13.2 or later, Android : 10.0 or later)

Exclusion criteria

Exclusion criteria: (1) Subjects with food allergies or hypersensitivities (2) Subjects with diseases that require constant medication, or with a medical history of severe diseases that require constant medication (3) Subjects who have been diagnosed with medical or surgical diseases that require hospitalization in the past 3 months (4) Subjects with disorders or taking medicine related to digestion or absorption of nutrients (5) Subjects with a medical history of diabetes, or have been used hypoglycemic agents or insulin for treatment of diabetes or related disorders (6) Subjects who have been diagnosed with glucose tolerance disorders in the past year (7) Subjects who are participating in another trial, have participated in the past 4 weeks, or plan to participate in another trial during the scheduled study period (8) Females who plan to have pregnancy or lactation (9) Subjects judged to be inadequate by the questionnaire of lifestyles (10) Subjects judged to be unsuitable for the study for other reasons by the investigator

Design outcomes

Primary

MeasureTime frame
Interstitial fluid glucose

Countries

Japan

Contacts

Public ContactMariko Ozawa

LaViena Inc. -

info@laviena.me03-6821-1389

Outcome results

None listed

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