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Effects of Canola Oil and Coconut Oil on Postprandial Metabolism in Older Adults With Increased Cardiometabolic Risk

Acute Effects of Canola Oil Compared With Coconut Oil on Postprandial Metabolism in Women and Men With Increased Risk for Cardiometabolic Diseases

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05208346
Enrollment
30
Registered
2022-01-26
Start date
2022-03-09
Completion date
2022-10-18
Last updated
2025-04-29

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

Conditions

Cardiovascular Diseases, Metabolic Syndrome

Keywords

Postprandial metabolic events

Brief summary

The aim of this study is to investigate the postprandial effects of fat content and fatty acid composition of mixed meals on parameters associated with cardiometabolic diseases. Therefore, older subjects with increased risk of cardiometabolic diseases consume 4 mixed meals with 25 or 50 g of either canola or coconut oil. In a postprandial period of 6 hours, outcomes associated with cardiometabolic risk (e.g., triglycerides) are analyzed.

Detailed description

In a crossover design, 30 older men and women with increased risk of cardiometabolic diseases consume 4 mixed meals, enriched with either 25 or 50 g canola or coconut oil. During a postprandial period of 6 hours, parameters of lipid metabolism (e.g., plasma triglycerides), glucose metabolism (e.g., plasma glucose, serum insulin), as well as markers of inflammation (e.g., IL-6), vascular system (e.g., pulse wave velocity) and antioxidant system (e.g., trolox equivalent antioxidative capacity) are analyzed. Furthermore, fatty acid profile, neuropsychologic parameters (e.g., attention), subjective feeling of hunger and satiety, and satiety-associated hormones (e.g., ghrelin) are assessed. Each intervention arm will be separated by a washout period of about 14 days.

Interventions

DIETARY_SUPPLEMENTMixed meals

Mixed meals enriched with either 25 or 50 g of canola or coconut oil

Sponsors

Union for the Promotion of Oil and Protein Plants (UFOP, Germany)
CollaboratorUNKNOWN
University of Bonn
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
60 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* BMI: 27 - 34,9 kg/m2 * Waist circumference: women ≥ 80 cm, men ≥ 94 cm * At least two of the following criteria of metabolic syndrome: Fasting triglycerides in serum: ≥ 150 mg/dl Fasting HDL-Cholesterol in serum: women \< 50 mg/dl, men \< 40 mg/dl Systolic blood pressure: ≥ 130 mmHg, diastolic blood pressure: ≥ 85 mmHg Fasting glucose in plasma: ≥ 100 mg/dL

Exclusion criteria

* Smoking * Diseases that may impact outcome measures (e.g., thyroid diseases, insulin-dependent diabetes mellitus, impaired renal function, tumors, anemia) * Intake of immunosuppressives or supplements (e.g., fish oil) * Participation in another study

Design outcomes

Primary

MeasureTime frameDescription
Parameters of glucose metabolism in blood IIPostprandial period of 6 hoursMeasurement of insulin (nmol/L)
Parameters of lipid metabolism in blood IVPostprandial period of 6 hoursMeasurement of HDL cholesterol (mg/dl)
Parameters of lipid metabolism in blood IPostprandial period of 6 hoursMeasurement of triglycerides (mg/dl)
Parameters of lipid metabolism in blood IIPostprandial period of 6 hoursMeasurement of total cholesterol (mg/dl)
Parameters of lipid metabolism in blood IIIPostprandial period of 6 hoursMeasurement of LDL cholesterol (mg/dl)
Parameters of lipid metabolism in blood VIPostprandial period of 6 hoursMeasurement of free fatty acids (mmol/L)
Parameters of glucose metabolism in blood IPostprandial period of 6 hoursMeasurement of glucose (mg/dl)

Secondary

MeasureTime frameDescription
Assessment of hunger and satietyPostprandial period of 6 hoursAssessment via visual analogue scales (e.g., 0 = not hungry at all, 10 = very hungry)
Assessment of gut hormonesPostprandial period of 6 hoursMeasurement of gut hormones associated with hunger and satiety in blood (ghrelin in pg/ml; PYY in pg/ml)
Assessment of attention and memoryPostprandial period of 6 hoursAssessment via validated neuropsychological questionnaires (paper-pencil)
Postprandial endothelial functionPostprandial period of 6 hoursAssessment via the Vicorder device (e.g., measurement of pulse wave velocity in m/s)
Postprandial inflammationPostprandial period of 6 hoursMeasurement of parameters of inflammation in blood (e.g., IL-6 in pg/ml)
Antioxidant systemPostprandial period of 6 hoursMeasurement of parameters of antioxidant system in blood (e.g., TEAC in mmol Trolox equivalents/L)
Fatty acid profilePostprandial period of 6 hoursAnalysis of fatty acid profile in serum (e.g., alpha-linolenic acid in µmol/L)

Countries

Germany

Outcome results

None listed

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