Investigation of Blood Glucose and Insulin Response After Intake of Vitalose

N/ACompletedNCT04596709

Beneo-Institute13 enrolled

Overview

The aim of this study is to assess the postprandial glucose and insulin response of Vitalose.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

DOUBLE

Enrollment

Conditions

Healthy Adults

Interventions

VitaloseDIETARY_SUPPLEMENT

dissolved in water

isomaltuloseDIETARY_SUPPLEMENT

dissolved in water

sucroseDIETARY_SUPPLEMENT

dissolved in water

glucose

Eligibility

Sex: ALLMin age: 18 YearsMax age: 50 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * healthy adults * Age 18-50 years * BMI ≥18.5 and ≤30.0 kg/m² Exclusion Criteria: * acute or chronic disease * food allergy or intolerance * intake of medications which affect glucose tolerance

Locations (1)

BioTeSys GmbH

Esslingen am Neckar, Germany

Outcomes

Primary Outcomes

2h iAUC for pp glucose response

Time frame: Baseline, 15, 30, 45, 60, 90, 120 minutes

2h iAUC for pp insulin response

Time frame: Baseline, 15, 30, 45, 60, 90, 120 minutes

Data from ClinicalTrials.gov

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