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Comparative test of the amount of food component absorbed depending on the time of intake

Comparative test of the amount of food component absorbed depending on the intake time of day (morning, midday or evening): open-label, crossover trial - Comparative test of the amount of food component absorbed depending on the intake time of day (morning, midday or evening)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056398
Enrollment
36
Registered
2025-01-13
Start date
2025-01-13
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

A single ingestion of the test food (200 mL) at morning. A single ingestion of the test food (200 mL) at midday. A single ingestion of the test food (200 mL) at evening.

Sponsors

KAGOME CO., LTD.
Lead Sponsor
CPCC Company Limited
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy people aged 20 to 39 years. 2. Who agree to participate in the trial and have completed a medical interview and pre-test.

Exclusion criteria

Exclusion criteria: 1. Whose body mass index (BMI) is less than 18.5 or above 25. 2. Who have a history of major surgery on the digestive system (except appendicitis). 3. Who visit the hospital for treatment of illnesses or receiving medication. 4. Lactating, pregnant or planning to be pregnant during this trial. 5. Who have allergic reaction to test foods. 6. Smokers (who have smoked within the last 6 months). 7. Who have irregular lifestyles, such as shift workers and late-night workers. 8. Who are not in the habit of eating three meals a day (breakfast, lunch and dinner) regularly. 9. Who consume vegetable or vegetable-fruit drinks on a daily basis (approx. three times a week or more). 10. Who have given blood in the last six months. 11. Who have difficulty having blood drawn. 12. Who have participated in other human trials within one month. 13. Who are judged unsuitable for this trial by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Area under the food component concentration curve (AUC) in the serum triglyceride-rich lipoprotein fraction after ingestion of the test food and the change of AUC.

Secondary

MeasureTime frame
Concentration of the food component in the serum triglyceride-rich lipoprotein fraction after ingestion of the test food and the change from before ingestion.

Countries

Japan

Contacts

Public ContactHayato Ouchi

Seishukai Clinic, Seishukai Medical corporation Clinical trial division

h-ouchi@seishukai.or.jp03-5827-0930

Outcome results

None listed

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