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Verification of emission effects of hazardous substances by ingestion of test foods

Verification of emission effects of hazardous substances by ingestion of test foods - Verification of emission effects of hazardous substances by ingestion of test foods

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040434
Enrollment
5
Registered
2020-12-25
Start date
2020-01-27
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 individuals

Interventions

Oral consumption of the test food for 24 weeks

Sponsors

Square Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Men and women between 20 and 64 years of age 2) Applicants who have a thorough understanding of the purpose and content of the examination and who have volunteered freely and agreed to participate in the examination in writing

Exclusion criteria

Exclusion criteria: 1) Those with serious diseases of the liver, kidney, heart, lung, digestive system, blood, endocrine system, and metabolic system 2) Those who have a disease requiring regular medication or a history of a serious disease requiring medication treatment 3) Those with a BMI of 26 or more 4) A person who regularly uses functional foods and supplements that may affect the discharge of hazardous substances 5) Those whose working hours are irregular due to night shift or irregular work 6) A person who smokes excessively or is a regular user of alcohol 7) Those whose lifestyle habits, such as eating and sleeping, are extremely irregular 8) Those who have donated blood within 4 weeks before obtaining consent 9) A person who has a history of hypersensitivity to test food ingredients 10) Those who are pregnant, lactating, or who intend to become pregnant during the examination period 11) Those who are participated in other clinical trials and monitored studies within one month prior to obtaining consent 12) Any other person deemed unsuitable as a subject by the study physician or study assignment physician

Design outcomes

Primary

MeasureTime frame
Urine test (TOX test), Mycotoxin, heavy metal test, organic acid test

Secondary

MeasureTime frame
Hematological tests, blood biochemistry tests, urinalysis, subjective quality of life questionnaires

Countries

Japan

Contacts

Public ContactAyaka Nakashima

euglena Co., Ltd. R&D department Functionality Research Section

nakashima@euglena.jp03-3453-4907

Outcome results

None listed

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