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

Not Applicable
Conditions
Healthy male subjects
Registration Number
JPRN-UMIN000026198
Lead Sponsor
Research Center for Immunological Analysis, Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Male
Target Recruitment
80
Inclusion Criteria

Not provided

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
serum uric acid level (at 2-3 weeks and 1 day before the intervention, and after 4, 8, 12 weeks of daily intake.)
Secondary Outcome Measures
NameTimeMethod
blood test, urinalysis (at 2-3 weeks and 1 day before the intervention, and after 4, 8, 12 weeks of daily intake.)
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