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Investigation on change with time of blood polyphenol concentration after its oral administration

Investigation on change with time of blood polyphenol concentration after its oral administration - Investigation on change with time of blood polyphenol concentration after its oral administration

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000030619
Enrollment
8
Registered
2019-04-01
Start date
2017-12-15
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

Normal healthy subjects

Interventions

Intake of plant polyphenol

Sponsors

SAPPORO HOLDINGS Ltd. Frontier Laboratory for Value Creation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Persons who have full ethical and regulatory approval and themselves and parental guardian give written informed consent 2.Healthy men and women who have serum uric acid value less than 8.0 mg / dL, and have never suffered a gout symptom 3.Healthy Japanese over 20 years old

Exclusion criteria

Exclusion criteria: 1.Persons receiving medications such as uric acid levels, hypertension, diabetes, etc. 2.Persons who are allergic to the test food 3.Pregnancy, breast-feeding, or pregnancy planning person 4.Those who are scheduled to undergo surgery / hospitalization, etc. for two months before and after the examination period (November 2017 to February 2018) 5.Persons who are judged unsuitable for participating in this trial by the principal investigator

Design outcomes

Primary

MeasureTime frame
Concentration of serum polyphenol

Secondary

MeasureTime frame
serum uric acid, creatinine, LDL cholesterol level, HDL cholesterol level, neutral fat, total cholesterol level, blood glucose level

Countries

Japan

Contacts

Public ContactShuichi Segawa

SAPPORO HOLDINGS Ltd. Frontier Laboratory for Value Creation

Syuuichi.segawa@sapporoholdings.co.jp054-629-7982

Outcome results

None listed

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