Ireland
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Starting soon Not applicable

SUVY VerSus SAccharose (SUVISA)

NCT07901491 · tracked via the Priya Life Science France tracker
Sponsor
Minerais SAS
Phase
Not applicable
Started
2026-11-09
Last updated
2026-10-28

Condition(s) studied

Healthy VolunteersErythritol

Investigational drug(s) / intervention(s)

SÜVYSucrose

SÜVY: Single oral dose of 50 g SÜVY, a proprietary ingredient consisting of a single fixed formulation of erythritol (E968) and polydextrose (E1200), administered as one product, dissolved in 250 mL still water.

Sucrose: Single oral dose of 50 g sucrose dissolved in 250 mL still water.

Study summary

Sugar substitutes are increasingly used to reduce sugar intake. SÜVY is a food ingredient combining erythritol and polydextrose. This study compares the blood sugar response, insulin response, and platelet activity after drinking a solution of SÜVY (50 g) versus a solution of regular sugar (sucrose, 50 g) in 14 healthy adults. Each participant takes part in two visits separated by at least 7 days, receiving one product per visit in random order. The goal is to evaluate whether SÜVY produces a lower blood sugar response than sucrose, and whether it has any effect on blood clotting markers.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy adult volunteers aged 18 to 50 years * Body Mass Index (BMI) between 18.5 and 29.5 kg/m² * Fasting blood glucose \< 1.10 g/L * HbA1c \< 6.0% * Non-smoker * No known hemostatic disorder or thrombotic history * No antiplatelet, anticoagulant or NSAID medication within 10 days prior to each visit * Able to provide written informed consent Exclusion Criteria: * Diabetes mellitus (type 1 or type 2) or any antidiabetic treatment * Known intolerance to polyols or irritable bowel syndrome * Pregnancy or breastfeeding * Chronic inflammatory disease * Participation in another clinical study within 3 months prior to inclusion * Any condition that, in the investigator's judgment, would compromise the participant's safety or the integrity of the study data

Primary outcome measure(s)

  • Incremental Area Under the Curve (iAUC) for Blood Glucose and Insulin — 0 to 120 minutes after oral ingestion
    Incremental area under the curve (iAUC) for blood glucose and insulin concentrations measured from T0 to T+120 minutes after oral ingestion of SÜVY or sucrose, calculated by the trapezoidal method. Blood samples collected at T0, T+15, T+30, T+45, T+60, T+90 and T+120 minutes.

Trial sites (1)

FacilityCityRegionStatus
Centre d'Investigation Clinique - CHU de Rennes - Hôpital Pontchaillou Rennes Ille-et-Vilaine
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07901491 on ClinicalTrials.gov ↗ ← All trials in France