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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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