Evaluation of the effects of aseptic-packaged low-protain cooked rice helping to responce moderately to postprandial blood glucose level on postprandial blood glucose and insulin levels in subjects with borderline type 2 diabetes melitus

Evaluation of the effects of aseptic-packaged low-protain cooked rice helping to responce moderately to postprandial blood glucose level on postprandial blood glucose and insulin levels in subjects with borderline type 2 diabetes melitus - Evaluation of the effects of packed low-protain boiled rice helping to response moderately to postprandial blood glucose level on postprandial blood glucose and insulin levels

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000021372

Enrollment

Registered

2016-03-07

Start date

2016-03-07

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 with impaired fasting glucose (fasting plasma glucose, 110-125 mg/dl) or with impaired glucose tolerance (120 minutes glucose level in 75g-OGTT, 140 - 199 mg/dl))

Interventions

Test food: aseptic-packaged low-protain cooked rice, 140g Control food: aseptic-packaged Niigata Koshihikari cooked rice, 148g

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1.Fasting plasma glucose levels are from 110 to 126 mg/dl or 2 minutes glucose levels in 75g-oral glucose tolerance test (OGTT) are from 140 to 200 mg/dl. 2.Volunteers being able to make self-judgent to particupate in this study and giving written informed consent. 3.Volunteers having screening test results judged to be appropriate for this study by investigator.

Exclusion criteria

Exclusion criteria: 1.Volunteers having severe history of the diseases (liver,kidney,hert,blood) judged to be inappropriate for this study. 2.Volunteers received gastrectomy,enterectomy,and gastro-intestinal dedeases,judged to be inappropriate for this study. 3.Diabetes mellitus. 4.Subjects who use oral medication affecting blood glucose. 5.Volunteers rejected participating in this study by chief investigater.

Design outcomes

Primary

Measure	Time frame
Time-dependent changes in postprandial plasma glucose levels	—

Secondary

Measure	Time frame
Time-dependent changes in postprandial insulin and incretin levels	—

Countries

Japan

Contacts

Public ContactNiigata Bio-Research Park, Inc

Niigata Bio-Research Park, Inc Business promotion division

nbrp-food-navi@nbrp.co.jp0250-25-1196

Outcome results

None listed

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