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Possible Pharmacological Effect of Quercetin in the Management of Hyperuricemia - Results From Real-life Clinical Studies

Possible Pharmacological Effect of Quercetin in the Management of Hyperuricemia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06652035
Enrollment
161
Registered
2024-10-22
Start date
2021-09-01
Completion date
2023-06-15
Last updated
2024-10-29

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

Conditions

Hyperuricemia

Brief summary

Quercetin, a natural flavonoid found in various fruits and vegetables, has gained attention for its potential role in managing hyperuricemia. Emerging evidence suggests that quercetin may reduce plasma uric acid levels by inhibiting xanthine oxidase, an enzyme responsible for uric acid production. Additionally, its anti-inflammatory and antioxidant properties could help mitigate the oxidative stress and inflammation associated with hyperuricemia. As a result, quercetin supplementation offers a promising avenue for therapeutic intervention in conditions like gout and other uric acid-related disorders.

Detailed description

In the present retrospective cross-sectional observational study, the investigators assessed the potential pharmacological effect of supplemental quercetin on the plasma uric acid levels of health adults. These participants visited nutritional clinics in Italy during the Coronavirus disease (COVID-19) pandemic for general health check-up in real-life to enhance their immune system with supplements aimed at providing additional protection against COVID-19 infection. The supplements, either quercetin or probiotic Streptococcus salivarius K12 (BLIS K12), were advised randomly to the participants for 90 days, tailored to individual needs and in the absence of any pre-defined criteria.

Interventions

DIETARY_SUPPLEMENTQuevir® (Quercetin Phytosome®)

500 mg Quevir® (Quercetin Phytosome®) tablet

DIETARY_SUPPLEMENTBactoblis®

Probiotic Streptococcus Salivarius K12 (ATCC BAA-1024)

Sponsors

The University of Urbino Carlo Bo, Italy
CollaboratorUNKNOWN
Liaquat University of Medical & Health Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy adults * BMI between 18.5 and 29.9 kg/m² * Non-smoker * Consumtion of less than 3 units of alcohol per day

Exclusion criteria

* \- Plasma uric acid concentrations above 7 mg/dL * Diagnosis of endocrinological, metabolic, oncological, neurological, or bowel inflammatory disease diseases, gout, kidney stones

Design outcomes

Primary

MeasureTime frameDescription
Change in plasma uric acid level90 daysSupplement effect on plasma uric acid level

Secondary

MeasureTime frameDescription
Change in plasma triglycerides level90 daysSupplement effect on plasma triglycerides level
Change in plasma glucose level90 daysSupplement effect on plasma glucose level
Change in plasma insulin level90 daysSupplement effect on plasma insulin level
Change in plasma creatine phosphokinase level90 daysSupplement effect on plasma creatine phosphokinase level
Change in alanine transaminase level90 daysSupplement effect on liver function
Change in plasma cholesterol level90 daysSupplement effect on plasma cholesterol level
Change in alkaline phosphatase level90 daysSupplement effect on liver function
Change in gamma-glutamyl transferase level90 daysSupplement effect on liver function
Change in bilirubin level90 daysSupplement effect on liver function
Incidence of side effects90 daysNumber of patients reporting side effects
Change in aspartate aminotransferase level90 daysSupplement effect on liver function

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026