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A randomized, double-blind, placebo-controlled, parallel-group study to investigate the hypouricemic effect of anserine ingestion

A randomized, double-blind, placebo-controlled, parallel-group study to investigate the hypouricemic effect of anserine ingestion - Hypouricemic effect of anserine ingestion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000028718
Enrollment
80
Registered
2017-08-19
Start date
2017-08-20
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 adult

Interventions

Ingestion of supplement containing anserine for 12 weeks Ingestion of placebo without anserine for 12 weeks

Sponsors

KSO Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Healthy males and females aged 20 to 64 years old 2.Individuals whose serum uric acid are from 5.5 mg/dL to 7.0 mg/dL 3.Individuals who can make self-judgment and are voluntarily giving written informed consent

Exclusion criteria

Exclusion criteria: 1.Individuals who use medications affecting uric acid metabolism 2.Individuals who cannot stop using supplements and/or functional foods affecting serum uric acid 3.Individuals who contract hyperuricemia needing treatment 4.Individuals who have a history of gout or are under treatment of gout 5. Individuals who have drinking habit more than 60 g in terms of pure alcohol a day for more than 5 days a week 6. Individuals who cannot stop drinking from 2 days before visit 7. Individuals who have a history of food allergy 8. Individuals who are under treatment or have a history of disease e.g., serious hyperlipidemia, diabetes, kidney disease, liver disease, or heart disease., thyroid disease, adrenal disease, or metabolic diseases 9. Individuals who use a medicine 10. Individuals who have chronic disease and regularly use medicines 11. Individuals who have a history of gastroenterological disease or operation on digestive organ 12.Individuals who are judged as unsuitable for the study because of the result of blood chemistry and hematology test at screening test 13.Individuals who have donated blood components and/or blood a volume of 200 mL and over within one month prior to the current study 14. Individuals who have under treatment or a history of drug addiction and/or alcoholism 15.Individuals who are planning to participate or already participating in other clinical studies 16.Individuals who are judged as unsuitable for the study by the investigator for other reasons

Design outcomes

Primary

MeasureTime frame
Serum uric acid at 4-week, 8-week, 12-week consumption

Secondary

MeasureTime frame
Uric acid excretion in the urine, 8-OHdG in the urine, questionnaire of daily habit, SF-8 and visual analogue scale to evaluate fatigue severity

Countries

Japan

Contacts

Public ContactEiji Yoshikawa

KSO Corporation Sales department

yoshikawa@kso.co.jp03-3452-7733

Outcome results

None listed

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