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Test of suppression of postprandial blood glucose elevation by food ingestion

Test of suppression of postprandial blood glucose elevation by food ingestion - Test of suppression of postprandial blood glucose elevation by food ingestion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057599
Enrollment
20
Registered
2025-04-15
Start date
2025-04-14
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

Single intake of bitter melon and foods containing corosolic acid Single intake of placebo foods containing corosolic acid

Sponsors

Lifix Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Male and female subjects aged 20 to 64 years (2) Normal to slightly elevated fasting blood glucose level (125 mg/dL or less) at baseline (3) Subjects who give written voluntary consent to participate in the study

Exclusion criteria

Exclusion criteria: (1) Those who have been diagnosed with diabetes and are currently undergoing treatment (2) Those who are currently taking medication for diabetes or high blood pressure (3) Those who are currently taking the test food or health food (4) Those who regularly take supplements related to cholesterol, blood pressure, blood lipids, or blood sugar levels (5) Those with serious diseases or mental disorders of the following systems: sugar metabolism, lipid metabolism, liver function, kidney function, heart, circulatory system, respiratory system, endocrine system, immune system, or nervous system. Those with a history of such diseases or disorders (6) Those who have been found to have abnormal clinical test values and are judged to have problems participating in the study (7) Those with diseases that are currently being treated or who have a history of serious diseases that required medication treatment (8) Those who may develop allergies in relation to the study (9) Those who are judged to be unsuitable as subjects based on the results of the lifestyle questionnaire (10) Those who are participating in other clinical research at the start of this study (11) Those who are pregnant or plan to become pregnant or breastfeed during the study period (12) Those who are judged to be unsuitable for participation in the study by the principal investigator (or the person in charge of conducting the study)

Design outcomes

Primary

MeasureTime frame
Changes in postprandial blood glucose levels

Secondary

MeasureTime frame
Changes in postprandial insulin

Countries

Japan

Contacts

Public ContactShigefumi Nibun

EAS inc. Clinical Trial Session

info@eas-ct.jp070-5415-3051

Outcome results

None listed

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