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Double-blind, placebo-controlled study for the effects of quercetin-rich gold-onion powder on vascular endothelial function.

Double-blind, placebo-controlled study for the effects of quercetin-rich gold-onion powder on vascular endothelial function. - Effects of quercetin-rich onion powder on vascular endothelial function.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014970
Enrollment
10
Registered
2014-08-27
Start date
2012-08-01
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

vascular endothelial dysfunction

Interventions

Ingesting 6 g of quercetin-rich gold-species onion powder daily for 4 weeks. Ingesting 6 g of ordinary onion powder daily for 4 weeks.

Sponsors

Hokkaido Information University
Lead Sponsor
Okamoto Plant Breeding Co. Ltd.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subjects who agree to participate in the current study with a written informed consent.

Exclusion criteria

Exclusion criteria: (1) Subjects who are pregnant or under lactation, or ones who would be expected to be pregnant during the study. (2) Subjects with unusually high and/or low blood pressure, or with abnormal hematological data, or abnormal urine test data. (3) Subjects who are under medication or receive treatment for chronic ailments (especially cancer, cardiovascular disease, diabetes, dyslipidemia, hypertension etc.) (4) Subjects who regularly use drugs (especially blood coagulation inhibitor, drugs to treat diabetes, drugs to treat dyslipidemia, antihypertensive drugs etc.) (5) Subjects with a history of allergy to medicine and food, especially onions (6) Heavy smokers and alcohol addicts, or subjects with irregular food habits. (7) Subjects who are suffering from severe cardiac disease, liver disease, renal disease, gastrointestinal disease etc. (8) Subjects who have undergone major surgery such as gastrectomy, gastrointestinal suture surgery, intestinal resection or any majo surgery in the digestive system. (9) Subjects with serious anemia. (10) Subjects who have blood coagulation disorders. (11) Subjects who are suspected of acute infectious disease morbidity such as influenza. (12) Subjects who donate 400ml whole blood within 12 weeks or who donate 200ml whole blood within 4 weeks or who donate plasma or platelets within 2 weeks prior to this study. (13) Subjects who are presently participating in other clinical trials. (14) Subjects who are not eligible due to physician's judgment.

Design outcomes

Primary

MeasureTime frame
Fasting and post-prandial effect on FMD (flow-mediated vasodilation)

Secondary

MeasureTime frame
Body composition (weight, BMI, fat percentage, abdominal circumference, blood pressure), blood lipids (T-cho, TG, LDL-cho, HDL-cho, VLDL-cho) blood glucose (FBG, HbA1c), blood coagulation system (platelet aggregation, PT, APTT, thrombotest), high sensitivity CRP (hsCRP), VAS questionnaire (fatigue, sleep, defecation frequency etc.)

Countries

Japan

Contacts

Public ContactDir. Prof. Jun Nishihira, M.D.

Hokkaido Information University Health Information Science Center

nishihira@do-johodai.ac.jp011-385-4411

Outcome results

None listed

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