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临床试验/NCT06591767
NCT06591767已完成不适用

Potential Pharmacological Effects of Supplemental Quercetin in the Management of Mild to Moderate Hyperuricemia

Liaquat University of Medical & Health Sciences1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2023年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
64
试验地点
1
主要终点
Effect on circulatory uric acid

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged between 18 and 75 years.
  • Diagnosed with obesity.
  • Diagnosed with hypercholesterolemia.
  • With or without moderate hyperuricemia (serum uric acid ≥ 8 mg/dL).
  • No restrictions on BMI, alcohol consumption, or smoking habits.

排除标准

  • Current use of uric acid-lowering medications (e.g., allopurinol, febuxostat).
  • Diagnosed with oncological diseases.
  • Diagnosed with neurological diseases.
  • Diagnosed with inflammatory bowel diseases.

结局指标

主要结局

Effect on circulatory uric acid

时间窗: 90 days

Change in plasma uric acid level

次要结局

  • Effect on body internal organs muscles(90 days)
  • Supplement safety and tolerability(90 days)
  • Effect on lipids(90 days)
  • Effect on glycemia(90 days)
  • Effect on liver function(90 days)

研究者

发起方
Liaquat University of Medical & Health Sciences
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Amjad Khan

Professor of Clinical Biochemistry and Experimental Medicine

Liaquat University of Medical & Health Sciences

研究点 (1)

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