Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| University of Urbino "Carlo Bo" | OTHER |
Not provided
Not provided
Not provided
Not provided
Uric acid, a metabolic byproduct of purine degradation in humans, is a known risk factor for conditions such as gout and type 2 diabetes. Research has shown that supplementation with quercetin can significantly reduce plasma uric acid levels in individuals with mild hyperuricemia, potentially mitigating these associated risks.
Uric acid, a metabolic byproduct of purine degradation in humans, is a significant risk factor for the development of gout and type 2 diabetes. Supplementation with quercetin, a flavonol not naturally produced by the human body, has been shown to significantly reduce plasma uric acid levels in individuals with mild hyperuricemia. This effect is primarily achieved through the inhibition of xanthine oxidoreductase, an enzyme crucial to uric acid production.
Quercetin is the most abundant polyphenol found in fruits and vegetables and is widely used as a dietary supplement to boost the immune system and promote overall health. It is characterized by three key properties: antioxidant, anti-inflammatory, and immunomodulatory. These combined actions make quercetin a promising candidate for supporting various health conditions where oxidative stress, inflammation, and immune function play a role, including cardiovascular health, healthy aging, bone and joint health, sports and physical activity, gut health, and respiratory well-being.
The above-described properties of quercetin prompted investigators to explore its potential uricosuric therapeutic effect in two clinical studies. The first study will assess this effect in a retrospective cohort of COVID-19 patients who received quercetin as a supplemental therapy. In the second study, its potential uricosuric therapeutic effect will be assessed in a randomized controlled prospective clinical trial involving patients with mild to moderate hyperuricemia.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Quercetin group | Experimental | In this group hyperuricemic patients (uric acid > 8 mg/dL) received oral supplemental Quercetin, twice a day for 90 days. |
|
| Control group 1 | Active Comparator | In this group hyperuricemic patients (uric acid > 8 mg/dL) received oral supplemental Berberine and monacolins based supplement, twice a day for 90 days. |
|
| Control group 2 | Active Comparator | In this group normouricemic patients (uric acid < 7 mg/dL) received oral supplemental Berberine and monacolins based supplement, twice a day for 90 days. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Quercetin | Dietary Supplement | 200 mg supplemental Quercefit® |
|
| Measure | Description | Time Frame |
|---|---|---|
| Effect on circulatory uric acid | Change in plasma uric acid level | 90 days |
| Measure | Description | Time Frame |
|---|---|---|
| Effect on lipids | Change in plasma cholesterol level | 90 days |
| Effect on lipids | Change in plasma triglycerides level | 90 days |
Not provided
Inclusion criteria:
Exclusion criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| S. Orsola-Malpighi Polyclinic Hospital | Bologna | Italy |
Not provided
| ID | Term |
|---|---|
| D033461 | Hyperuricemia |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
Not provided
| ID | Term |
|---|---|
| D011794 | Quercetin |
| ID | Term |
|---|---|
| D044948 | Flavonols |
| D005419 | Flavonoids |
| D002867 | Chromones |
| D001578 | Benzopyrans |
| D011714 |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Berberol K® | Combination Product | Berberine Phytosome® 730 mg + MonakoPure® containing 2.9 mg of monacolin K and KA from red yeast rice extract |
|
| Effect on glycemia | Change in plasma glucose level | 90 days |
| Effect on glycemia | Change in plasma insulin level | 90 days |
| Effect on body internal organs muscles | Change in the Creatine Phosphokinase (CPK) levels | 90 days |
| Effect on liver function | Change in the Alanine Aminotransferase levels | 90 days |
| Effect on liver function | Change in the Aspartate Aminotransferase levels | 90 days |
| Effect on liver function | Change in the Alkaline Phosphatase levels | 90 days |
| Effect on liver function | Change in the Gamma-Glutamyl Transferase levels | 90 days |
| Effect on liver function | Change in the Bilirubin levels | 90 days |
| Supplement safety and tolerability | Number of patients reporting possible side effects | 90 days |
| Pyrans |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |