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临床试验/NCT07377097
NCT07377097尚未招募不适用

Effects of Sweetener Consumption on Risk Factors for Heart Disease

Charite University, Berlin, Germany0 个研究点目标入组 80 人开始时间: 2026年1月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
80
主要终点
Change of glucose tolerance

研究概览

简要总结

The aim of this prospective interventional study is to investigate the metabolic effects of consuming artificial and natural sweeteners in persons with prediabetes. Prediabetes is a condition characterized by blood sugar levels that are elevated above normal but not yet meeting the criteria for type 2 diabetes. This condition markedly increases the risk of progressing to type 2 diabetes, which in turn can lead to complications including cardiovascular diseases.

Artificial sweeteners such as saccharin and sucralose, as well as natural sugar substitutes like erythritol, are increasingly used as alternatives to sugar and are recommended for individuals at cardiometabolic risk - including overweight individuals, patients with prediabetes, or diabetics - to help reduce caloric intake. Recent literature has reported possible negative associations between artificial sweeteners and blood sugar regulation in healthy subjects (1). Additionally, effects on various blood cells have been observed. For example, erythritol has been shown to alter platelet function leading to increased reactivity in healthy study participants following consumption (2).

However, the impact of alternative sweeteners on metabolic processes and their effects on blood coagulation in patients with prediabetes-a population at increased risk-has not been systematically studied. In this planned interventional study, 80 patients meeting laboratory criteria for prediabetes will be randomly assigned to one of four groups, each receiving a different intervention for two weeks: saccharin, sucralose, erythritol, or a control group receiving water. The doses reflect the acceptable daily intake or known doses that are considered safe.

After enrollment, participants will visit the study center 2 times: before starting the intervention and after completing the intervention. During these visits, biological samples such as blood, urine, and stool will be collected to study metabolism, gut bacteria, immune and blood cell function. Tests will include an oral glucose tolerance test, coagulation tests, and additional blood analyses. Additionally, participants will wear a glucose monitor to track blood sugar fluctuations during the intervention.

The investigators hypothesize that consumption of alternative sweeteners negatively affects blood sugar regulation and insulin sensitivity in patients with prediabetes. Furthermore, this study will explore how the candidate sweeteners influence the gut microbiome, blood cells and other metabolic factors in this population.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

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

  • Presence of prediabetes (HbA1c 5.7-6.4% or glucose after oral glucose tolerance test 140 to 199 mg/dL)
  • Written informed consent available

排除标准

  • Inability to communicate sufficiently in the required language
  • Dementia or other significantly cognitively impairing condition
  • Current pregnancy or breastfeeding
  • Other severe internal, neurological, or psychiatric condition
  • History of gout
  • History of gallstones / diagnosis of cholelithiasis

研究组 & 干预措施

Saccharin Group

Active Comparator

Intervention: Saccharin

干预措施: Saccharin (Dietary Supplement)

Sucralose Group

Active Comparator

Intervention: Sucralose

干预措施: Sucralose (Dietary Supplement)

Erythritol Group

Active Comparator

Intervention: Erythritol

干预措施: Erythritol (Dietary Supplement)

Control Group

Placebo Comparator

Intervention: Vehicle

干预措施: Vehicle (Dietary Supplement)

结局指标

主要结局

Change of glucose tolerance

时间窗: Baseline vs. within 1 week after intervention

Measured by AUC of oral glucose tolerance test

次要结局

  • Change of microbiome(Baseline vs. within 1 week after intervention)
  • Flow cytometry analysis of changes in frequency of circulating monocyte subsets (%)(Baseline vs. within 1 week after intervention)
  • Flow cytometry analysis of changes in platelet activation marker expression (% positive platelets)(Baseline vs. within 1 week after intervention)
  • Flow cytometry analysis of changes in platelet activation marker expression (MFI)(Baseline vs. within 1 week after intervention)
  • Changes in lipid profile(Baseline vs. within 1 week after intervention)
  • Changes in blood metabolite profiles by liquid chromatography / mass spectrometry(Baseline vs. within 1 week after intervention)
  • Changes in body mass index (BMI)(Baseline vs. within 1 week after intervention)
  • Changes in waist to hip ratio (WHR)(Baseline vs. within 1 week after intervention)
  • Changes in body fat percentage(Baseline vs. within 1 week after intervention)

研究者

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

Marco Witkowski

Marco Witkowski, MD, PhD

Charite University, Berlin, Germany

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