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Effect of supplement containing dihydroquercetin on Insulin Resistance in Obesity -A randomized, double-blind, and parallel group study-

Effect of supplement containing dihydroquercetin on Insulin Resistance in Obesity -A randomized, double-blind, and parallel group study- - Effect of supplement containing dihydroquercetin on Insulin Resistance

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000018418
Enrollment
60
Registered
2015-07-24
Start date
2015-07-25
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

Healty volunteer

Interventions

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

Sponsors

KSO Corporation
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1)Japanese males aged 30 to 64 years old. 2)Subjects whose BMI are from 25 to 40 kg/m2 3)Subjects whose HOMA-R are higher than 1.6 and ISI level is low. 4)Subjects who can make self-judgment and are voluntarily giving written informed consent

Exclusion criteria

Exclusion criteria: 1)Subjects who use oral medication affecting blood glucose. 2)Subjects who constantly use supplements and/or functional foods (including Food for Specified Health Uses, Food with function claims) affecting blood glucose. 3)Subjects who have declared allergic reaction to ingredients contained in test diets. 4) Subjects who are diabetes (including those who are treated with insulin administration) 5)Subjects who contract or are under treatment or are medical history for serious diseases (e.g.,liver disease, kidney disease, and/or heart disease), thyroid gland disease, adrenal gland disease, and/or metabolic disorder. 6)Subjects who have a chronic disease and use medicines continuously. 7)Subjects who have a history of digestive disease affecting digestion and absorption. 8) Subjects whose fasting blood glucose are above 140 mg/dl. 9)Subjects who are judged as unsuitable for the study based on the results of blood tests by the investigator. 10)Subjects who have donated over 200 mL of blood and/or blood components within the last one month prior to the current study or over 400 mL of blood and/or blood components within the last three months prior to the current study. 11)Subjects who are diagnosed as anemic and not suitable for frequent collection of blood. 12)Subjects who are under treatment for or have a history of drug addiction and/or alcoholism. 13)Subjects who are planning to participate in other clinical studies. 14)Subjects who are judged as unsuitable for the study by the investigator for other reasons.

Design outcomes

Primary

MeasureTime frame
ISI(Matsuda Index)

Secondary

MeasureTime frame
HOMA-R, HOMA-beta, glucose, insulin, AUC of glucose and insulin, QUICKI

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