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Effect of Sweetness Intensity of a Sucrose Solution on Blood Glucose Regulation and Energy Intake

Einfluss Der Süßintensität Einer Saccharose-Lösung Auf Die Blutglukoseregulation Und Energieaufnahme in Gesunden Männern

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04991714
Enrollment
30
Registered
2021-08-05
Start date
2021-08-05
Completion date
2022-12-30
Last updated
2023-01-26

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

Conditions

Blood Glucose, Low, Hunger

Brief summary

The aim of the present study is to investigate the influence of the modulation of the sweetness intensity of a carbohydrate (sucrose)-containing solution on metabolic effects, in particular the regulation of blood glucose concentration and regulation of hunger & satiety.

Detailed description

The study is designed as a randomised cross-over intervention study with four interventions. The study investigates the influence of sweetness modulation by Rebaudioside M (sweetness enhancement) and Lactisol (sweetness inhibition) of a 10% sucrose solution, corresponding to the concentration of a regular soft drink, on blood glucose regulation (blood glucose concentration and regulating hormones) in healthy male volunteers. Furthermore, the study assesses ad libitum energy intake, individual feelings of hunger and satiety, metabolic responses to the interventions, and preference for sweet-tasting foods such as sugar and sweeteners. In addition, the participants' individual thresholds for sweet taste, as well as morphological markers for taste sensitivity and body composition will be recorded as potential influencing factors.

Interventions

sweet taste inhibitor (decreases sweetness)

DRUGRebaudioside M

Sweetener (increases sweetness)

OTHERSucrose

10% Sucrose corresponding to a regular soft drink

Sponsors

University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* male * healthy * non-smoking * normal taste responses towards sweet taste

Exclusion criteria

* female * regular smokers * disturbed glucose and/or lipid metabolism * regular intake of medication * known allergies against one of the test compounds * ageusia * alcohol or drug addiction * intake of antibiotics within the past 2 months

Design outcomes

Primary

MeasureTime frameDescription
Blood glucose concentrationover a time span of 120 minutes after drinking the test solutionGlucose concentration \[mg/dL\] in plasma samples before, and 15, 30, 60, 90, and 120 minutes after drinking the test solution
Insulin concentrationover a time span of 120 minutes after drinking the test solutionInsulin concentration \[mmol/L\] in plasma samples before, and 15, 30, 60, 90, and 120 minutes after drinking the test solution
GLP-1 concentrationover a time span of 120 minutes after drinking the test solutionGlucagon-like peptide 1 concentration in plasma samples \[mmol/L\] before, and 15, 30, 60, 90, and 120 minutes after drinking the test solution
GIP-concentrationover a time span of 120 minutes after drinking the test solutionGastric inhibitory polypeptide concentration in plasma samples \[mmol/L\] before, and 15, 30, 60, 90, and 120 minutes after drinking the test solution

Secondary

MeasureTime frameDescription
Food intake120 minutes after drinking of the test solutionAd libitum Food intake from a standardized breakfast
Metabolic changesover a time span of 120 minutes after drinking the test solutionMetabolome analysis in plasma samples \[mmol/L\] before, and 15, 30, 60, 90, and 120 minutes after drinking the test solution

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026