Effects of Functional Ingredients in an Acute Metabolic Challenge Context

NCT02623608 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2019-08-22

No results posted yet for this study

Summary

After an energy-rich meal the blood levels of glucose and lipids undergo a marked temporary increase, triggering a wave of oxidative stress due to the appearance of excess free radicals in adipose and muscle tissues. Elevated postprandial hypertriglyceridemia has been associated with increased risk of cardiovascular disease and type 2 diabetes. Hence, postprandial changes in different circulating biomarkers are potential predictors of cardiometabolic risk. In addition to the possibility of evaluating acute variations in metabolic risk markers in response to different types of fat, the metabolic challenge approach may serve as a challenge-meal background in order to reveal possible beneficial effects of specific food ingredients. In this study, circulating cardiometabolic disease-related biomarkers, including endotoxemia, will be assessed postprandially in search for beneficial actions of particular functional food ingredients consumed in combination with a high-fat meal.

Conditions

  • Metabolic Syndrome

Interventions

OTHER

Reference breakfast

A high fat, high calorie breakfast

OTHER

Active Ingredient 1

A high fat, high calorie breakfast including the Active Ingredient 1

OTHER

Active Ingredient 2

A high fat, high calorie breakfast including the Active Ingredient 2

OTHER

Active Ingredient 3

A high fat, high calorie breakfast including the Active Ingredient 3

OTHER

Active Ingredient 4

A high fat, high calorie breakfast including the Active Ingredient 4

Sponsors & Collaborators

  • Vinnova

    collaborator OTHER_GOV
  • Antidiabetic Food Centre AFC

    collaborator UNKNOWN
  • Lund University

    lead OTHER

Principal Investigators

  • Juscelino Tovar, PhD · Lund University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2015-08-31
Primary Completion
2016-01-31
Completion
2016-07-31

Countries

  • Sweden

Study Locations

More Related Trials

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 NCT02623608 on ClinicalTrials.gov