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Ability of Grape Seed Proanthocyanidins to Reduce Postprandial Triglycerides in Humans

Ability of Grape Seed Proanthocyanidins to Reduce Postprandial Triglycerides in Humans

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01688154
Enrollment
16
Registered
2012-09-19
Start date
2013-02-28
Completion date
2013-06-30
Last updated
2013-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Function, Triglyceride Metabolism

Brief summary

Grape seed proanthocyanidins have been reported to possess a hypotriglyceridemic effect after an acute or chronic consumption in rodents. In this study, we aimed to investigate the effects of an acute consumption of proanthocyanidins before a breakfast meal in humans. Moreover, the mechanisms implicated in the reduction of plasma triglycerides levels by grape seed proanthocyanidins in humans should be elucidated as well as its activity on vascular function.

Detailed description

The intervention will consist in the administration of 2 capsules containing the grape seed proanthocyanidins extract or 2 empty capsules (placebo) just before breakfast, which will consist of 100g of white bread, 75g of salami, 50g of fatty cheese, 125g of yogurt (10% fat), 25ml of olive oil and water ad libitum. The nutritional composition of this meal is as follows: 1.200 Kcal of energy content, 15% of energy from proteins, 22% from carbohydrates and 63% from fat (35% saturated fat), and 120mg of cholesterol. Blood samples will be taken at point 0.5,1,2,3 and 6 hours after breakfast. Moreover, urine samples will be collected at time 0 and 6 hours.

Interventions

DIETARY_SUPPLEMENT35 mg/Kg of grape seed proanthocyanidins extract (2 capsules)
OTHER2 empty capsules

Sponsors

University Rovira i Virgili
CollaboratorOTHER
Hospital Universitari Sant Joan de Reus
CollaboratorOTHER
Technological Centre of Nutrition and Health, Spain
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults between the ages of 20 and 40 * Signing the informed consent

Exclusion criteria

* Body mass index (BMI) lower than 18.5 or greater than 27 Kg/m2 * Smokers * Regular medication * Consumption of medication during the last week * Following a weight-loss diet * Vegetarians * Abnormal glucose levels * Diabetes * Cardiovascular disease * Gastrointestinal disease * Anemia * Nuts allergy

Design outcomes

Primary

MeasureTime frame
Area under the curve of plasma triglycerides concentration0-180 minutes

Secondary

MeasureTime frame
Endothelial function (assessed by ischemic reactive hyperemia)0-0.5-1-2-3-6 hours
Blood lipid levels, markers of inflammation and oxidation0-0.5-1-2-3-6 hours
Plasma levels of procyanidins metabolites0-0.5-1-2-3-6 hours
Blood pressure0-0.5-1-2-3-6 hours
Membrane lipid composition of erythrocytes and oxidation markers.0-0.5-1-2-3-6 hours
Non-targeted metabolomics and 8-epi-prostaglandin-F2α levels (in urine)0-6 hours
Markers of cholesterol metabolism in PBMCs (mRNA and protein).0-0.5-1-2-3-6 hours

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026