Fructose and (Aging)
FRUage
Investigation of the Effect of Fructose on Health Parameters and the Intestinal Barrier in Healthy Individuals
1 other identifier
interventional
32
1 country
1
Brief Summary
The aim of the present study is to investigate the effect of fructose consumption on health parameters and the intestinal barrier in healthy individuals
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2026
CompletedFirst Submitted
Initial submission to the registry
April 30, 2026
CompletedFirst Posted
Study publicly available on registry
August 11, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2027
August 11, 2026
April 1, 2026
1.2 years
April 30, 2026
August 5, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Changes in markers of intestinal permeability
Changes in concentrations of bacterial endotoxin in blood plasma
At the end of the treatment (1 month)
Cytokine release from blood immune cells stimulated with bacterial toxins
Changes in cytokine concentration in supernatant of immune cells before and after the treatments
At the end of the treatment (1 month)
Study Arms (2)
Fructose
EXPERIMENTALFollowing a standardization of their nutritional intake for three days, participants will receive a drink supplemented with free fructose.
Glucose
EXPERIMENTALFollowing a standardization of their nutritional intake for three days, participants will receive a drink supplemented with free glucose.
Interventions
Following a standardization of their nutritional intake for three days, participants will either receive a drink supplemented with low doses of free fructose (5%).
Following a standardization of their nutritional intake for three days, participants will either receive a drink supplemented with low doses of free glucose (5 %).
Eligibility Criteria
You may qualify if:
- all gender, healthy collective ≥ 18 years old
You may not qualify if:
- 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
- Smoking
- Liver diseases
- Renal insufficiency
- Rheumatoid arthritis
- COPD with ≥ 2 exacerbations per year
- Chronic pancreatitis or recurrent acute pancreatitis
- +3 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Vienna
Vienna, 1090, Austria
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Prof. Dr.
Study Record Dates
First Submitted
April 30, 2026
First Posted
August 11, 2026
Study Start
April 1, 2026
Primary Completion (Estimated)
July 1, 2027
Study Completion (Estimated)
December 1, 2027
Last Updated
August 11, 2026
Record last verified: 2026-04