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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03159065
Other study ID # InVeg (1)
Secondary ID
Status Completed
Phase N/A
First received May 17, 2017
Last updated May 18, 2017
Start date September 2014
Est. completion date January 2015

Study information

Verified date May 2017
Source Lund University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Consumption of polyphenol-rich fruits and vegetables may improve the postprandial glucose and insulin responses and hence promote well-being. It has previously been observed that consumption of a bilberry drink decreases the postprandial insulin demand. In the present study, the impact of probiotic fruit beverages with different polyphenol profiles on the postprandial levels of glucose and insulin, were investigated.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date January 2015
Est. primary completion date November 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Healthy, not on medication, non-allergic, individuals aged 18-65 years old, having a BMI between 20-30 kg/m2 and also maintaining stable body weight, i.e. less than 5% weight change in the last three months before the study.

Exclusion Criteria:

Study Design


Intervention

Other:
Bilberry
Fruit beverage with bilberry and fermented oatmeal
Blackcurrant
Fruit beverage with blackcurrant and fermented oatmeal
Mango
Fruit beverage with mango and fermented oatmeal
Beetroot
Fruit beverage with beetroot and fermented oatmeal
Rose hip
Fruit beverage with rose hip and fermented oatmeal
Glucose drink
A reference glucose drink

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Lund University

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy of the study products on the postprandial serum insulin The postprandial incremental area under the curve for serum insulin Incremental area under the curve for serum insulin from 0 min up to 120 min following the ingestion of the study product
Secondary Efficacy of the study products on the postprandial serum glucose The postprandial incremental area under the curve for serum glucose Incremental area under the curve for serum glucose from 0 min up to 120 min following the ingestion of the study product
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