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Effect of ingestion of trial supplement on serum uric acid level -A double blind, placebo controlled study-

Effect of ingestion of trial supplement on serum uric acid level -A double blind, placebo controlled study- - Effect of ingestion of trial supplement on serum uric acid level

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000023663
Enrollment
40
Registered
2016-08-19
Start date
2016-08-21
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 male subject

Interventions

Ingestion of trial supplement A for 4 weeks Ingestion of trial supplement B for 4 weeks Ingestion of trial supplement C for 4 weeks Ingestion of placebo for 4 weeks

Sponsors

FANCL Corporation
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1) Japanese males aged from 20 to less than 65 years old. 2) Subjects whose serum uric acid levels are included within 6.0mg/dL and 8.0mg/dL.

Exclusion criteria

Exclusion criteria: 1) Subjects who are under treatment or have a history of hyperuricemia or gout. 2) Subjects who have a history of gouty arthritis or gouty arthritis. 3) Subjects who are under treatment or have a history of rheumatoid arthritis. 4) Subjects who have a history of urinary stone or kidney stone. 5) Subjects who has a disease under treatment or are judged to that medical treatment are necessary by the doctor 6) Subjects who have under treatment or history of disease such as diabetes, liver disease, kidney disease, heart disease, adrenal cortex disease. 7) Subjects who are routinely use the health food, dietary supplement, and medicine including over-the-counter drug for improving of serum uric acid. 8) Subjects who routinely use or are planned to use analgesics (non-steroidal analgesics, steroidal analgesics, etc.). 9) Subjects with allergies to the products used in the study. 10) Subjects who are planned to change their lifestyle. 11) Subjects who have participated in other clinical study within the last one month prior to the current study 12) Subjects who are judged as unsuitable for the study by the investigator for other reason

Design outcomes

Primary

MeasureTime frame
Serum uric acid level

Secondary

MeasureTime frame
Urine uric acid level Subgroup analysis using SNP Relationship among serum uric acid, urine uric acid, and SNP

Countries

Japan

Contacts

Public ContactYoshiki Shimizu

FANCL CORPORATION Research institute

shimizu_yoshiki@fancl.co.jp045-820-3755

Outcome results

None listed

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