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Effects of Prebiotics on GLP-1 in Type 2 Diabetes

University of Oslo (UIO) logo

University of Oslo (UIO)

Status

Completed

Conditions

Diabetes Type 2

Treatments

Dietary Supplement: Maltodextrin
Dietary Supplement: Prebiotic fibers: oligofructose and inulin

Study type

Interventional

Funder types

Other

Identifiers

NCT02569684
1180 REK

Details and patient eligibility

About

The aim of the study is to compare the effects of prebiotics versus placebo on blood concentrations of glucagon-like peptide-1 in subjects with diabetes type 2.

Full description

We looked at 6 weeks supplementation with a prebiotic fibre mix of inulin and FOS. Cross over design compared to maltodextrin as placebo. Additional outcome measures: blood glucose, insulin, GLP-2, ghrelin, PYY and leptin after a standardized mixed meal test. Also measured changes in microbiota composition and SCFA in feces before and after intervention/placebo periods, and subjective measures of appetite.

Enrollment

37 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diabetes type 2
  • BMI 18,5 - 40
  • Not medicated with insulin, GLP-1 analogues or DPP4 inhibitors
  • Moderate intake of alcohol
  • Not excessive exercise
  • Less than 3 kg weight change the last two months
  • Intake of less than 30 g dietary fiber per day

Exclusion criteria

  • IBD
  • IBS
  • Coeliac disease
  • Have used antibiotics within the last two months
  • Have used supplements with prebiotics or probiotics the last two months
  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

37 participants in 2 patient groups, including a placebo group

Arm A
Active Comparator group
Description:
Prebiotic fibers: Oligofructose and inulin
Treatment:
Dietary Supplement: Prebiotic fibers: oligofructose and inulin
Arm B
Placebo Comparator group
Description:
Maltodextrin
Treatment:
Dietary Supplement: Maltodextrin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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