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

Completed
Conditions
Hyperuricemia
Registration Number
NCT06652035
Lead Sponsor
Liaquat University of Medical & Health Sciences
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
161
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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in plasma uric acid level90 days

Supplement effect on plasma uric acid level

Secondary Outcome Measures
NameTimeMethod
Change in alanine transaminase level90 days

Supplement effect on liver function

Change in aspartate aminotransferase level90 days

Supplement effect on liver function

Change in alkaline phosphatase level90 days

Supplement effect on liver function

Change in gamma-glutamyl transferase level90 days

Supplement effect on liver function

Change in bilirubin level90 days

Supplement effect on liver function

Incidence of side effects90 days

Number of patients reporting side effects

Change in plasma insulin level90 days

Supplement effect on plasma insulin level

Change in plasma creatine phosphokinase level90 days

Supplement effect on plasma creatine phosphokinase level

Change in plasma cholesterol level90 days

Supplement effect on plasma cholesterol level

Change in plasma triglycerides level90 days

Supplement effect on plasma triglycerides level

Change in plasma glucose level90 days

Supplement effect on plasma glucose level

Trial Locations

Locations (1)

Dr. Buccomino Medical Clinic

🇮🇹

Milano, Italy

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