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Clinical Study on the Effects of Short-Term Fructose Intake on Metabolic Indicators and Gut Microbiota in Obese and Healthy Individuals

Clinical Study on the Effects of Short-Term Fructose Intake on Metabolic Indicators and Gut Microbiota in Obese and Healthy Individuals

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111816
Enrollment
Unknown
Registered
2025-11-06
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Interventions

Obesity placebo:Same volume of pure water (placebo, 300 mL, to be consumed within 2 minutes)
Control placebo:Same volume of pure water (placebo, 300 mL, to be consumed within 2 minutes)
Obesity fructose:A single dose of high-fructose beverage (fructose solution, dose 0.75 g/kg, 300 mL, consumed within 2 minutes).
Control fructose:A single dose of high-fructose beverage (fructose solution, dose 0.75 g/kg, 300 mL, consumed within 2 minutes).

Sponsors

Shanghai Fengxian District Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Healthy Participants: 1.Age: 18–45 years; both genders eligible, able to comprehend and sign the informed consent form. 2.Body Mass Index (BMI): 18.5–24 kg/m^2. 3.No prior history of diabetes, severe cardiovascular, hepatic/renal diseases, or mental disorders. Obese Participants: 1.Age: 18–45 years; both genders eligible; able to understand the study protocol and voluntarily sign the informed consent form. 2.Body Mass Index (BMI): >=28.0 kg/m^2[12]. Metabolic Status: 3.May have simple obesity or metabolic abnormalities (e.g., fasting blood glucose 6.1–7.0 mmol/L or postprandial 2-hour glucose 7.8–11.1 mmol/L, but not meeting diabetes diagnostic criteria). 4.Health Status: No prior history of diabetes, severe cardiovascular, hepatic/renal diseases, or mental disorders.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1.History of alcohol addiction or recent heavy drinking; pregnant or breastfeeding women; 2.Allergy or intolerance to the trial beverage components; 3.Recent use (within 3 months) of antibiotics, probiotics, or other treatments altering gut microbiota; 4.Any other circumstances deemed unsuitable by the investigator.

Design outcomes

Primary

MeasureTime frame
Blood metabolic indicators (glucose, insulin, triglycerides, uric acid, liver function, etc.);

Countries

China

Contacts

Public ContactZhang Shan

Shanghai Fengxian District Central Hospital

shanzhang_168@163.com+86 185 0174 1665

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026