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Evaluation of the effects of melinjo seed extract powder on the level of serum uric acid.

Evaluation of the effects of melinjo seed extract powder on the level of serum uric acid. - Evaluation of the effects of melinjo seed extract powder on the level of serum uric acid.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000026342
Enrollment
20
Registered
2018-07-01
Start date
2017-02-28
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

hyperuricemia

Interventions

Oral administration of melinjo seed extract powder (300mg/day, 12weeks)

Sponsors

Research Center for Immunological Analysis, Inc.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: [1] Male subjects whose serum uric acid level is between 7.0 mg/dL and 7.9 mg/dL, and age is between 20 and 69 years old.

Exclusion criteria

Exclusion criteria: [1] Taking drugs that may affect serum uric acid level. [2] Individuals who can't stop taking supplement and functional food that may affect serum uric acid level during the test peripd. [3] Individuals who have an infection needed systemic therapy. [4] Individuals who are considered that participation for this trial is difficult because of psychiatric symptoms or psychosis. [5] Individuals who have a uncontrollable diabetes millutus or requiring administration of insulin. [6] Individuals who are sensitive to test products. [7] AST >150U/L. [8] ALT >150U/L. [9] Total bilirubin >2.0mg/dL. [10] Individuals who have a kidney disease. [11] Individuals who have or had a severe allergy or asthma. [12] Individuals who have a disease needing immediate treatment or serious complication. [13] Individuals with a digestive organ disease or surgical history having an influence on digestive absorption. [14] Individuals who have an anamnesis or a history of present illness of drug dependence or alcohol dependence. [15] Individuals who are participated in another clinical trial that intake/apply any of food, drug, and cosmetics, or willing to be that. [16] Individuals who suffer from gout. [17] Individuals judged inappropriate for participating the study by the principal

Design outcomes

Primary

MeasureTime frame
serum uric acid level (at 2-3 weeks and 1 day before the intervention, and after 4, 8, 12 weeks of daily intake.)

Secondary

MeasureTime frame
blood test, urinalysis (at 2-3 weeks and 1 day before the intervention, and after 4, 8, 12 weeks of daily intake.)

Countries

Japan

Contacts

Public ContactTatsuya Sakamoto

Research Center for Immunological Analysis, Inc. none

info@menekibunseki.com086-286-9333

Outcome results

None listed

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