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A Dose-response Study of Dietary Resveratrol on Lipid Metabolism Disorder

Department of Nutrition and Food Hygiene,School of Public Health, Sun Yat-sen University

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04886297
Enrollment
168
Registered
2021-05-14
Start date
2021-05-01
Completion date
2022-09-30
Last updated
2022-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dyslipidemias

Brief summary

In order to study the effect of resveratrol on the improvement of lipid and uric acid metabolism, randomized intervention trials were conducted to compare the effects of resveratrol on the improvement of lipid and uric acid metabolism in different dose groups. To explore the best dose of resveratrol for the prevention and treatment of metabolic diseases provide an important scientific basis.

Detailed description

In order to study the effect of resveratrol on the improvement of lipid and uric acid metabolism, randomized controlled trials were conducted to enrolled 160 patients with dyslipidemia. The subjects were divided into 0 mg / d, 100 mg / d, 300 mg / d, 600 mg/ d four dose groups, intervention for 8 weeks, comparing different doses of resveratrol on lipid and uric acid metabolism. To explore the best dose of resveratrol for the prevention and treatment of metabolic diseases provide an important scientific basis.

Interventions

DRUGMega Resveratrol® capsules

Subjects were orally administered Mega Resveratrol® capsules daily for 8 weeks.

DRUGMega Resveratrol® Placebo capsules

Mega Resveratrol® Placebo capsules

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
35 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Dyslipidemia * The age between 35 and 70 years old

Exclusion criteria

* Intake of any medicine that affect lipid metabolism currently or in the preceding 6 months * Dietary supplementation with phytochemicals including resveratrol in the preceding 3 months * History of acute or chronic infectious disease, autoimmune disease, cancer, traumatic injury, or surgery in the preceding 1 month * History of severe chronic disease including AS and CVD, liver or renal dysfunction, and lactation or pregnancy * Pregnant woman and Breast Feeding Women

Design outcomes

Primary

MeasureTime frameDescription
Effect of resveratrol on lipid profile in patients with dyslipidemiaChange from Baseline to 4 weeks and 8 weeksLipid profile in serum will be measured, mainly including TC, TG, LDL-C and HDL-C, by automatic biochemical analyzer.

Secondary

MeasureTime frameDescription
Effect of resveratrol on uric acid and xanthine oxidase in patients with dyslipidemiaChange from Baseline to 4 weeks and 8 weeksUric acid concentration and xanthine oxidase activity will be measured by automatic biochemical analyzer and commercial kits, respectively.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026