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NCT04596709 Clinical Trial

Investigation of Blood Glucose and Insulin Response After Intake of Vitalose

Healthy Adults Clinical Trial

Official title:
Investigation of Blood Glucose and Insulin Response After Intake of Vitalose and Isomaltulose in Comparison to Sucrose and Glucose

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04596709
Other study ID # BTS1586/20
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 22, 2020
Est. completion date December 1, 2020

Study information
Verified date December 2020
Source Beneo-Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 13
Est. completion date December 1, 2020
Est. primary completion date December 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Dietary Supplement:
• Vitalose
dissolved in water
• isomaltulose
dissolved in water
• sucrose
dissolved in water
• glucose
dissolved in water

Locations
Country Name City State
Germany BioTeSys GmbH Esslingen

Sponsors (2)
Lead Sponsor Collaborator
Beneo-Institute BioTeSys GmbH

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary 2h iAUC for pp glucose response Baseline, 15, 30, 45, 60, 90, 120 minutes
Primary 2h iAUC for pp insulin response Baseline, 15, 30, 45, 60, 90, 120 minutes
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