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Investigation of Blood Glucose and Insulin Response After Intake of Vitalose

NCT04596709 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 13

Last updated 2020-12-07

No results posted yet for this study

Summary

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

Conditions

  • Healthy Adults

Interventions

DIETARY_SUPPLEMENT

Vitalose

dissolved in water

DIETARY_SUPPLEMENT

isomaltulose

dissolved in water

DIETARY_SUPPLEMENT

sucrose

dissolved in water

DIETARY_SUPPLEMENT

glucose

dissolved in water

Sponsors & Collaborators

  • BioTeSys GmbH

    collaborator OTHER

  • Beneo-Institute

    lead INDUSTRY

Principal Investigators

  • Daniel Menzel, Dr. · BioTeSys GmbH

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-10-22
Primary Completion
2020-12-01
Completion
2020-12-01

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04596709 on ClinicalTrials.gov