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临床试验/NCT04316390
NCT04316390已完成不适用

Influence of Hesperidin and Vitamin C on Uric Acid Concentration

University of Kiel2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2022年7月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Changes in uric acid serum concentrations

研究概览

简要总结

Aim of the study is to investigate the impact of hesperidin and/or vitamin C on elevated uric acid concentrations.

详细描述

Duration of the study is 9 weeks. 1) a washout week, 2) two intervention weeks, 3) four weeks washout period, 4) two intervention weeks.

The study is conducted under free living conditions. During washout weeks consumption of orange juice or citrus fruits or vitamin C containing supplements is restricted.

During intervention weeks 200 mL of study drink is consumed daily. And participants are asked to maintain their normal physical activity and habitual diet. Additional citrus or vitamin C containing beverages are not allowed.

At the beginning and the end of each intervention phase uric acid, insulin sensitivity, blood pressure, pulse wave velocity and bioavailability of hesperidin are assessed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • higher uric acid concentration (≥5.5 mg/dL)
  • Informed written consent

排除标准

  • pregnancy
  • fructose intolerance
  • gout or medicated hyperuricemia
  • diabetes mellitus
  • antidiabetic or cytostatic medication
  • weight loss (≥5% in the past 3 months)
  • consumption of vitamin C-containing supplements
  • parallel participation in a clinical trial
  • anemia and / or iron deficiency

结局指标

主要结局

Changes in uric acid serum concentrations

时间窗: Baseline (pre) and post two weeks of intervention

measured via uric acid serum concentration (mg/dL)

次要结局

  • changes in pulse wave velocity(Baseline (pre) and post two weeks of intervention)
  • insulin sensitivity(Baseline (pre) intervention periods)
  • changes in uric acid excretion(Baseline (pre) and post two weeks of intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Dr. Dr. Anja Bosy-Westphal

Prof. Dr. Dr. Anja Bosy-Westphal

University of Kiel

研究点 (2)

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