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Study on the detection of nutrients in test foods and vegetables in blood

Study on the detection of nutrients in test foods and vegetables in blood - Study on the detection of nutrients in test foods and vegetables in blood

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000045952
Enrollment
10
Registered
2022-03-31
Start date
2021-11-02
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

Single intake of tstudy food (containing related ingredients 1000mg ) Single intake of control food substance

Sponsors

Miura Clinic, Medical Corporation Kanonkai
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Subjects of men and women aged 20 to 64 (2) Subjects who received a sufficient explanation of the purpose and contents of the study, an ability to consent, a volunteer who volunteered to participate with a good understanding and who agreed to participate in the study

Exclusion criteria

Exclusion criteria: (1)Subjects with liver disease, kidney disease, digestive system disease, heart disease, peripheral angiopathy and others who have a medical history that may affect the results of this test, or subjects who have a history of surgery (2)Subjects who show abnormal liver function and kidney function test values (3)Subjects who have a disease currently being treated (4)Subjects who have developed stone disease within the second degree of kinship (5)Subjects with food and drug allergy (6)Subjects taking warfarin (7)Subjects with anemic symptoms (8)Subjects on diet (9)Subjects with irregular lives (10)Subjects who can not quit the intake of health food (including food for FOSHU and Foods with Function Claims') and designated quasi-drugs during the test period (11)Subjects who are taking medication (OTC drugs, including prescription drugs) continuously (12)Subjects taking excessive alcohol (13)Subjects who cannot stop drinking from the day before the test to the day of the test (14)Subjects who are pregnant or who are planning pregnancy or breastfeeding during the study period (15)Subjects participating in or planning to participate in other clinical trials at the start of this study (16)Subjects judged by the investigator as inappropriate

Design outcomes

Primary

MeasureTime frame
Fe, Zn, Folic acid, VB1, VA, Alb, TP

Countries

Japan

Contacts

Public ContactMakoto Terashima

Oneness Support Co., Ltd. Clinical Trial Division

mterashima@oneness-sup.co.jp0648018917

Outcome results

None listed

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