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Clinical Trials in Canada / NCT03266055
Active, not recruiting Not applicable

Effects of Blueberry on Gut Microbiota and Metabolic Syndrome

NCT03266055 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2017-09-01
Last updated
2026-09-08

Condition(s) studied

Gut MicrobiotaMetabolic Syndrome

Investigational drug(s) / intervention(s)

50 g of blueberry powder, taken daily for 8 weeks50g of placebo blueberry powder, taken daily for 8 weeks

50 g of blueberry powder, taken daily for 8 weeks: Subjects will consume blueberry powder during 8 weeks to test the possible effects of blueberries on gut microbiota composition and on metabolic syndrome parameters.

50g of placebo blueberry powder, taken daily for 8 weeks: Subjects will consume blueberry placebo powder to test if there is a significant difference on the impact on gut microbiota composition and metabolic syndrome parameters between this treatment and the active treatment (blueberry powder).

Study summary

There is growing evidence that nutritional intervention with dietary polyphenols can positively modulate the gut microbiota to improve cardiometabolic health. Whether the beneficial effects of blueberries on obesity and the metabolic syndrome can be linked to their potential impact on the gut microbiota and intestinal integrity remains speculative at this time. Moreover, the mechanisms of action underlying health benefits associated to blueberry consumption are still unknown. The investigators are thus proposing to combine the study of metagenomics, transcriptomics and metabolomics to test whether a prebiotic activity of highbush blueberries can play a role in the prevention of obesity-linked metabolic syndrome in a clinical setting.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Men and premenopause women in good health * Caucasians * At least one of the following : BMI between 25 and 40 kg/m2 or Waist circumference ≥ 80 cm for women and ≥ 94 cm for men * At least one of the following : TG ≥ 1.35 mmol/L or fasting insulinemia ≥ 42 pmol/L Exclusion Criteria: * Metabolic disorders (hypertension, diabetes, hypercholesterolemia) * Regular use of medication affecting study parameters * Use of natural health product in the last 3 months * Use of antibiotics in the last 3 months * Nicotine users * Allergy or intolerance for blueberries * Blueberry taste aversion * More than 2 alcohol drinks par day * Particular dietary habits (vegetarism, gluten-free diet, cetogenic diet...) * Weight change of more than 5% in the last 3 months * Surgery in the last 3 months or planed during the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Laval University Québec Canada

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03266055 on ClinicalTrials.gov ↗ ← All trials in Canada