Investigation of Blood Glucose and Insulin Response After Intake of Vitalose

Beneo

Status: Completed

Conditions: Healthy Adults

Treatments: Dietary Supplement: sucrose; Dietary Supplement: isomaltulose; Dietary Supplement: glucose; Dietary Supplement: Vitalose

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT04596709

BTS1586/20

Details and patient eligibility

About

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

Enrollment: 13 patients

Sex: All

Ages: 18 to 50 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Double Blind

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13 participants in 4 patient groups, including a placebo group

Vitalose

Active Comparator group

Description:

dissolved in water

Treatment:

Dietary Supplement: Vitalose

isomaltulose

Active Comparator group

Description:

dissolved in water

Treatment:

Dietary Supplement: isomaltulose

sucrose

Placebo Comparator group

Description:

dissolved in water

Treatment:

Dietary Supplement: sucrose

glucose

Placebo Comparator group

Description:

dissolved in water

Treatment:

Dietary Supplement: glucose