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临床试验/NCT07757347
NCT07757347招募中不适用

Investigation of the Effect of Fructose on Health Parameters and the Intestinal Barrier in Healthy Individuals

University of Vienna1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2026年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
32
试验地点
1
主要终点
Changes in markers of intestinal permeability

研究概览

简要总结

The aim of the present study is to investigate the effect of fructose consumption on health parameters and the intestinal barrier in healthy individuals

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
Single (Participant)

入排标准

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

入选标准

  • all gender, healthy collective ≥ 18 years old

排除标准

  • Chronic inflammatory diseases of the gastrointestinal tract
  • Metabolic diseases or taking medication to treat metabolic diseases
  • Fructose malabsorption
  • Hereditary fructose intolerance
  • Food intolerances and/or allergies, as well as food allergies that require special dietary interventions
  • Special diets, such as vegetarian/vegan diets
  • Unstable body weight within the last 6 months (fluctuations of > 5%)
  • BMI < 19 kg/m2 & > 29,9 kg/m2
  • Bariatric surgery
  • Liver diseases
  • Renal insufficiency
  • Rheumatoid arthritis
  • COPD with ≥ 2 exacerbations per year
  • Chronic pancreatitis or recurrent acute pancreatitis
  • Alcohol consumption above 10 g/d for women and above 20 g/d for men
  • Pregnancy and breastfeeding
  • Viral or bacterial infections that occurred no longer than 3 weeks ago

研究组 & 干预措施

Glucose

Experimental

Following a standardization of their nutritional intake for three days, participants will receive a drink supplemented with free glucose.

干预措施: Glucose (Other)

Fructose

Experimental

Following a standardization of their nutritional intake for three days, participants will receive a drink supplemented with free fructose.

干预措施: Fructose (Other)

结局指标

主要结局

Changes in markers of intestinal permeability

时间窗: At the end of the treatment (1 month)

Changes in concentrations of bacterial endotoxin in blood plasma

Cytokine release from blood immune cells stimulated with bacterial toxins

时间窗: At the end of the treatment (1 month)

Changes in cytokine concentration in supernatant of immune cells before and after the treatments

次要结局

未报告次要终点

研究者

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

Prof. Dr. Ina Bergheim

Prof. Dr.

University of Vienna

研究点 (1)

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