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Investigation of Blood Glucose and Insulin Response After Intake of Vitalose

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04596709
Enrollment
13
Registered
2020-10-22
Start date
2020-10-22
Completion date
2020-12-01
Last updated
2020-12-07

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

Conditions

Healthy Adults

Brief summary

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

Interventions

DIETARY_SUPPLEMENTVitalose

dissolved in water

DIETARY_SUPPLEMENTisomaltulose

dissolved in water

DIETARY_SUPPLEMENTsucrose

dissolved in water

DIETARY_SUPPLEMENTglucose

dissolved in water

Sponsors

BioTeSys GmbH
CollaboratorOTHER
Beneo-Institute
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
2h iAUC for pp glucose responseBaseline, 15, 30, 45, 60, 90, 120 minutes
2h iAUC for pp insulin responseBaseline, 15, 30, 45, 60, 90, 120 minutes

Countries

Germany

Outcome results

None listed

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