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The verification for the time-dependent change of blood metabolites of the test food

The verification for the time-dependent change of blood metabolites of the test food: a crossover comparison trial - The verification for the time-dependent change of blood metabolites of the test food

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000047068
Enrollment
8
Registered
2022-03-03
Start date
2022-03-04
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 Japanese subjects

Interventions

Test food: (1) Test food A (2) Test food B Administration: &lt
Test food A&gt
After taking blood samples before intake, take test food A (270 mg) with water (100 mL) &lt
Test food B&gt
After taking blood samples before intake, take test food B (300 mg) with water (100 mL) *The intervention sequence is test food A to test food B, and each food is single ingestion.

Sponsors

Toyo Sugar Refining Co., Ltd.
Lead Sponsor
Medical Corporation Seishinkai, Takara Clinic University of Miyazaki
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Japanese 2. Male or female 3. Subjects aged 20 or more 4. Healthy subjects

Exclusion criteria

Exclusion criteria: 1. Subjects who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, and myocardial infarction 2. Subjects who have a pacemaker or an implantable cardioverter defibrillator (ICD) 3. Subjects currently undergoing treatment for any of the following chronic disease: cardiac arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 4. Subjects who take "Foods for Specified Health Uses", "Foods with Functional Claims", or other functional food/beverage in daily use 5. Subjects currently taking medicines (include herbal medicines) and supplements 6. Subjects who are allergic to medications and/or the test-food-related products 7. Subjects who are pregnant, breast-feeding, and planning to become pregnant 8. Subjects who suffer from COVID-19 9. Subjects who have been enrolled in other clinical trials within the last 28 days before the agreement to participate in this trial or plan to participate another trial during this trial 10. Subjects who are judged as ineligible to participate in the study by the physician

Design outcomes

Primary

MeasureTime frame
The area under the curve of blood metabolites concentration

Secondary

MeasureTime frame
The maximum blood concentration of metabolites, the measured values at each assessment point* of blood metabolites concentration, and metabolites concentration in 24-hour urine collection *It indicates before test-food consumption, at one, two, four, six, and 24 hours after test-food consumption

Countries

Japan

Contacts

Public ContactYushi Hashizume

Toyo Sugar Refining Co., Ltd. Research & Development Department

hashizume-y@toyosugar.co.jp03-3668-7874

Outcome results

None listed

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