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Pilot study of the effect of test drink in subjects with postprandial hyperglycemia.

Pilot study of the effect of test drink in subjects with postprandial hyperglycemia. - Examination of inhibitory effect of test drink on postprandial hyperglycemia.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031596
Enrollment
24
Registered
2018-03-05
Start date
2018-03-06
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

Intake of water (single ingestion) - washout period - beverage containing plant extract (single ingestion) Intake of beverage containing plant extract (single ingestion) - washout period - water (sing

Sponsors

TTC Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Healthy males and females from 20 to 64 years of age 2) Blood glucose level at postprandial 30 minitues is ranged from 130 mg/dL to 199 mg/dL 3) Priority is given to those with a blood glucose peak of 30 minutes

Exclusion criteria

Exclusion criteria: 1) Subjects who routinely use health food containing large amount of participating component or health food for diet 2) Subjects routinely taking medicine or health food which may influence glucose metabolism 3) Subjects who have body mass index (BMI) less than 18.5 kg/square meter or more than 30.0 kg/square meter 4) Subjects who have fasting blood glucose more than 126 mg/dL on preliminary examination 5) Subjects who has under treatment or a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) 6) Subjects having possibilities for emerging allergy related to the current study 7) Subjects who are under medication or having a history of serious diseases for which medication was required 8) Subjects who are judged as unsuitable for the current study based on the results of clinical and physical preliminary examination 9) Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study 10) Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating 11) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire 12) Subjects judged as unsuitable for the study by the investigator for other reasons

Design outcomes

Primary

MeasureTime frame
Postprandial blood glucose level, change of blood glucose level

Secondary

MeasureTime frame
Area under the curve of blood glucose level, maximum blood glucose level

Countries

Japan

Contacts

Public ContactShinsuke Tsuji

TTC Co., Ltd. Clinical Research Planning Department

s.tsuji@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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