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临床试验/NCT06420401
NCT06420401招募中不适用

Precision Treatment of Hyperuricemia Based on Different Combinations of Prebiotics

Sun Yat-sen University2 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2024年5月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
160
试验地点
2
主要终点
Change of excretion of uric acid

研究概览

简要总结

Hyperuricemia is a major risk factor for many chronic diesease. Recently, gut mcirobiota has been identified as a novel theraputic target for hyperuricemia. Both annimal studies and pilot human trials have demonstrated that administration of prebiotics help delay the progression of hyperuricemia throuh several mechanisms. This trial aims to examine its protective effects and potential mechanisms in clinical trials.

详细描述

Hyperuricemia is a major risk factor for many chronic diseases. Recently, dysbiosis of gut microbiota has been reported to play an important role in the pathogenesis of hyperuricemia. Animal studies have demonstrated that administration of prebiotics help delay the progression of hyperuricemia through several mechanisms such as reduction in endotoxemia, and enhanced production of short-chain fatty acids and hippuric acid.

However, whether administration of prebiotics also has a protective effect in subjects with hyperuricemia remain under-explored. Moreover, whether the original gut microbiota will influence the protective effect of prebiotics remains largely unknown.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Local residents aged between 18-80 years old;
  • Stable weight (<5% weight change over the past 3 months);
  • Fsating uric acid > 420 umol/L for male and > 360 umol/L for female on two different days;
  • Not taking uric acid lowering drugs or have stopped taking uric acid lowering drugs for over 4 weeks at the time of recruitment;
  • Absence of any diet or medication that might interfere with uric acid metabolims or gut microbiota, especially antibiotics, prebiotics or probiotics at the least 4 weeks before recruitment

排除标准

  • Acute illness or evidence of any acute or chronic inflammatroy of infective diseases;
  • Participation in regular diet program more than 2 times per week in the lastest 3 months prior to recruitment;
  • Mental illness rendering them unable to understand the nature, scope, and possible consequences of the study;
  • Women of childbearing age who are pregant, breast-feeding or preparing for pregnancy; patients who had surgey within the past 6 months or planned surgery during the trial period.

结局指标

主要结局

Change of excretion of uric acid

时间窗: from baseline to 12 weeks after intervention

excretion rate of uric acid assessed by secretion rate of uric acid in urine during 3 hours

Change of serum uric acid

时间窗: from baseline to 12 weeks after intervention

change of fasting uric acid level assessed by biochemical detector

次要结局

  • Change of gut microbiota(from baseline to 12 weeks after intervention)
  • Change of microbial metabolites(from baseline to 12 weeks after intervention)
  • Change in insulin sensitivity(from baseline to 12 weeks after intervention)
  • Change in waist circumference(from baseline to 12 weeks after intervention)
  • Change in lipid profiles(from baseline to 12 weeks after intervention)
  • Change in blood pressure(from baseline to 12 weeks after intervention)

研究者

发起方
Sun Yat-sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Min Xia

Professor

Sun Yat-sen University

研究点 (2)

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