Skip to main content
Clinical Trials/NCT03135041
NCT03135041
Completed
Not Applicable

Effects of a Combination of Prebiotic Fibres on Weight Loss During an Energy Restricted Diet in an Overweight/Obese Population

University of Copenhagen1 site in 1 country117 target enrollmentMay 26, 2017
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
University of Copenhagen
Enrollment
117
Locations
1
Primary Endpoint
Weight loss
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The aim of this study is to investigate whether a diet supplemented with two prebiotic fibres induces greater changes in body weight compared to placebo during 12 weeks of energy restriction in an obese/overweight population.

The hypothesis is that the fiber-containing dietary supplement will:

  1. Induce greater changes in body weight compared to the placebo group 2) change the gut microbiota composition 3) improve glucose homeostasis 4) decrease serum concentration of triglycerides, total and LDL cholesterol

The hypothesis is that the effect of the intervention on weight loss will be partly mediated by the diet-induced changes in the gut microbiota composition.

Detailed Description

Prebiotics are nutrients that specifically utilized by the gut microbiota. Beneficial health effects of prebiotics are generally attributed to 1) stimulation of beneficial bacteria and SCFA production, and consequently; improved barrier function, regulation of enteroendocrine peptide secretion and resistance to inflammatory stimuli; 2) modulation of lipid metabolism, possibly by suppression of lipogenic enzymes and thus decreased synthesis of lipoproteins and triglycerides; and 3) increased mineral absorption. Inulin is recognized as a common prebiotic. Fibersol-2 is a resistant starch that has been suggested to induce satiety, when given in a dose of 10 g. Intake of inulin has been shown to induce changes in the microbial abundance and increase production of SCFA19; whereas resistant starch has been shown to improve insulin sensitivity and postprandial glucose AUC20. However, the effects of an intervention with a combination of these two fibers on obesity and body composition during an energy restricted diet have not been addressed. Supplements with other types of fibres in addition to energy restriction have shown additional effects in weight reduction. In this study, the effects of a combination product of two prebiotic fibres on additional weight loss during energy restriction in a placebo-controlled, randomized parallel study with a duration of 12 weeks will be tested. Furthermore, the effects of the fibres on the gut microbial composition, markers of metabolic syndrome (MetS) and glucose metabolism will be tested. The active diet will contain intervention products high in dietary fibre and the placebo diet will contain maltodextrin. The fiber-containing dietary supplements will add approximately 20 g of prebiotic fibres per day, where approximately 10 g will be inulin and approximately 10 g will be resistant maltodextrin. The intervention products and placebo will be consumed as milk. The fiber-containing dietary supplement is expected to induce additional weight loss, compared to placebo and to affect the gut microbiome and markers of metabolic disease.

Registry
clinicaltrials.gov
Start Date
May 26, 2017
End Date
May 24, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Thomas Meinert Larsen

Associate Professor, PhD

University of Copenhagen

Eligibility Criteria

Inclusion Criteria

  • BMI: 28-45 kg/m2
  • Non-smoking
  • Haemoglobin level ≥7 mmol/L

Exclusion Criteria

  • Use of antibiotics three months prior to study and during the study. If a participant uses antibiotics prior to randomization, the participant will be invited to be re-screened 3 months after the last use of antibiotics, provided that it is realistic to complete the study no later than the scheduled LPLV
  • Weight change \>3 kg two months prior to study
  • Blood donation other than for this study \<1 month prior to study and during study.
  • Participation in clinical trials other than for this \<1 month prior to study and during study
  • Intensive physical training/ elite athlete (\>10 hours of strenuous physical activity per week)
  • Unstable medication for dyslipidaemia and elevated blood pressure (the participant must have had a stable dose in the three months prior to study start), and use of systemic glucocorticoids
  • Medication for T2D
  • Treatment with metformin
  • Dietary supplements with pro- and/or prebiotics and/or fibre 6 weeks prior to study
  • Special dietary regimen (vegetarians, vegans etc.), as evaluated by study staff

Outcomes

Primary Outcomes

Weight loss

Time Frame: Measurements will be performed at baseline and after 12 weeks of intervention

Differences in changes in body weight between the group that receives fiber-containing dietary supplement and placebo group

Secondary Outcomes

  • Body composition(Measurements will be performed at baseline and after 12 weeks of intervention)
  • Gut microbiota composition and function(Measurements will be performed at baseline and after 12 weeks of intervention)
  • Glucose metabolism(Measurements will be performed at baseline and after 12 weeks of intervention)
  • Lipid metabolism(Measurements will be performed at baseline and after 12 weeks of intervention)
  • Inflammatory markers(Measurements will be performed at baseline and after 12 weeks of intervention)
  • SCFA concentration(Measurements will be performed at baseline and after 12 weeks of intervention)
  • Lipidomics and bile acids(Measurements will be performed at baseline and after 12 weeks of intervention)
  • Metabolomics(Measurements will be performed at baseline and after 12 weeks of intervention)
  • Weight loss(Measurements will be performed at baseline and after 12 weeks of intervention)

Study Sites (1)

Loading locations...

Similar Trials