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Examination on a transition in a post-meal blood sugar level by three dietary methods(examination on soy first effects)

Examination on a transition in a post-meal blood sugar level by three dietary methods(examination on soy first effects) - Examination on a transition in a post-meal blood sugar level by three dietary methods(examination on soy first effects)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000030186
Enrollment
12
Registered
2017-12-01
Start date
2017-12-01
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

Healthy adult

Interventions

On the day intake of the two of warmed rice balls within 8 minutes. On the day intake of the two of warmed rice balls after finished eating the salad within 13 minutes. On the day intake of the two of

Sponsors

HUMA R&D CORP
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Age:30 and over, below 50. 2)Sex:Males and females with Japanese nationality. 3)BMI of 22 and over, below 25. 4)Consumption of carbohydrates in three meals a day.

Exclusion criteria

Exclusion criteria: 1)Currently in treatment with medication, or currently in exercise therapy and/or dietary therapy under medical supervision. 2)Previous history of hepatic disorder, severe kidney, endocrine, cardiovascular, gastrointestinal, pulmonary, hematological, or metabolic disorder, or a complication of these. 3)Arrhythmia or serious anemia. 4)Use of a coagulant. 5)Symptoms of dizziness, lightheadedness, palpitation, headache, breathlessness, etc. 6)Presence or previous history of hepatitis. 7)Current intake of a health food product or a supplement that has an influence on the blood sugar level. 8)Pregnant or nursing. 9)Presence or previous history of mental disorder (depression, etc.). 10)Presence or previous history of allergic reaction to medication or a food product. 11)Working on night shift or with alternative work schedule. 12)Participation in any other clinical study involving human subjects within 3 months or current participation in any other clinical study involving human subjects. 13)Subjects who are deemed to be unsuitable by the investigator.

Design outcomes

Primary

MeasureTime frame
1)Post-meal blood sugar level 2)Survey on fullness 3)AUC (Area Under Curve)

Countries

Japan

Contacts

Public ContactOchitani Daisuke

HUMA R&D CORP Clinical Development Division

ochitani@huma-c.co.jp81-3-3431-1260

Outcome results

None listed

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