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Completed

NCT Number: NCT05208346

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

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.

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Key information

Age range

60 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Bonn

Bonn, 53115, Germany

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Mixed meals

Dietary Supplement

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

Primary outcomes

  1. Parameters of lipid metabolism in blood I

    Time frame: Postprandial period of 6 hours

    Measurement of triglycerides (mg/dl)

  2. Parameters of lipid metabolism in blood II

    Time frame: Postprandial period of 6 hours

    Measurement of total cholesterol (mg/dl)

  3. Parameters of lipid metabolism in blood III

    Time frame: Postprandial period of 6 hours

    Measurement of LDL cholesterol (mg/dl)

  4. Parameters of lipid metabolism in blood IV

    Time frame: Postprandial period of 6 hours

    Measurement of HDL cholesterol (mg/dl)

  5. Parameters of lipid metabolism in blood VI

    Time frame: Postprandial period of 6 hours

    Measurement of free fatty acids (mmol/L)

  6. Parameters of glucose metabolism in blood I

    Time frame: Postprandial period of 6 hours

    Measurement of glucose (mg/dl)

  7. Parameters of glucose metabolism in blood II

    Time frame: Postprandial period of 6 hours

    Measurement of insulin (nmol/L)

Secondary outcomes

  1. Assessment of hunger and satiety

    Time frame: Postprandial period of 6 hours

    Assessment via visual analogue scales (e.g., 0 = not hungry at all, 10 = very hungry)

  2. Assessment of gut hormones

    Time frame: Postprandial period of 6 hours

    Measurement of gut hormones associated with hunger and satiety in blood (ghrelin in pg/ml; PYY in pg/ml)

  3. Assessment of attention and memory

    Time frame: Postprandial period of 6 hours

    Assessment via validated neuropsychological questionnaires (paper-pencil)

  4. Postprandial endothelial function

    Time frame: Postprandial period of 6 hours

    Assessment via the Vicorder device (e.g., measurement of pulse wave velocity in m/s)

  5. Postprandial inflammation

    Time frame: Postprandial period of 6 hours

    Measurement of parameters of inflammation in blood (e.g., IL-6 in pg/ml)

  6. Antioxidant system

    Time frame: Postprandial period of 6 hours

    Measurement of parameters of antioxidant system in blood (e.g., TEAC in mmol Trolox equivalents/L)

  7. Fatty acid profile

    Time frame: Postprandial period of 6 hours

    Analysis of fatty acid profile in serum (e.g., alpha-linolenic acid in µmol/L)

Sponsors and collaborators

Lead sponsor

University of Bonn

Other

Collaborators

  • Union for the Promotion of Oil and Protein Plants (UFOP, Germany)

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jan 26, 2022
Registry last updated
Apr 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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