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The effect of polymethoxy flavonoid on a liver function,sugar,lipid metabolism and obesity.Randomized Control Trial

The effect of polymethoxy flavonoid on a liver function,sugar,lipid metabolism and obesity.Randomized Control Trial - The study of effectiveness of Polymethoxy flavonoid

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021816
Enrollment
44
Registered
2016-04-08
Start date
2016-04-27
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

Borderline of Fatty liver

Interventions

One Capsule a day which contain 2mg of polymethoxy flavonoid One Capsule a day which contain no polymethoxy flavonoid

Sponsors

ARKRAY, Inc.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Japanese healthy volunteer (20<=age<75, male and female) 2)borderline of fatty liver 3)Those who are suitable for this trial by doctor decision. 4)Those Who can ingest the test food during the trial 5) Those who continue one's excise and/or diet therapy if needed. 6) Those who can give informed consent by the document.

Exclusion criteria

Exclusion criteria: 1)Viral hepatitis patient, alcoholic hepatitis patient, autoimmune liver damage patient 2)BMI>=30 3)Heart failure, myocardial infarction with a history of the past of the treatment 4)Those who takes medicine for antihypertensive drug, lipidosis symptom therapeutic drug, diabetes therapeutic drug, livers 5)Those who are under treatment for atrial fibrillation, arrhythmia, a liver damage, a renal damage, cerebrovascular disorder, rheumatism, diabetes, dyslipidemia, high blood pressure 5)Those who suffer any severe disease diagnosised by the responsible doctor. 6) Those who drink more than 20 grams alcohol a day everyday (beer 500 ml or sake around 1 go) 7) Those who takes a supplement regularly. 8) Those who have food allergy. 9) Those who is in breast-feeding or pregnancy, or wishes to become pregnant during the study period. 10) Those who had participated in a clinical trial within 30 days before a screening test. 11) Those who is judged as ineligible by principal investigators or researchers.

Design outcomes

Primary

MeasureTime frame
AST, ALT,gammaGTP,QOL

Secondary

MeasureTime frame
BMI, percent of body fat, girth of the abdomen, quantity of muscle, HOMA-IR, acylglycerol, total cholesterol HDL cholesterol, LDL cholesterol, blood sugar level, HbA1c, insulin, sLOX-1, cys-TTR, arteriosclerosis index, nonHDL cholesterol, genetic test,ferritin,type4-collagen7S

Countries

Japan

Contacts

Public ContactHirosato Kawakami

Karada Lab, Inc. The Director of the Laboratory

kawakamih@arkray.co.jp050-5536-5694

Outcome results

None listed

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