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

U

University of Bonn

Status

Completed

Conditions

Cardiovascular Diseases
Metabolic Syndrome

Treatments

Dietary Supplement: Mixed meals

Study type

Interventional

Funder types

Other

Identifiers

NCT05208346
528/191

Details and patient eligibility

About

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.

Full 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.

Enrollment

30 patients

Sex

All

Ages

60 to 80 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

30 participants in 4 patient groups

Canola oil high-fat
Experimental group
Description:
Participants randomized to receive a mixed meal with 50 g canola oil
Treatment:
Dietary Supplement: Mixed meals
Coconut oil high-fat
Experimental group
Description:
Participants randomized to receive a mixed meal with 50 g coconut oil
Treatment:
Dietary Supplement: Mixed meals
Canola oil low-fat
Experimental group
Description:
Participants randomized to receive a mixed meal with 25 g canola oil
Treatment:
Dietary Supplement: Mixed meals
Coconut oil low-fat
Experimental group
Description:
Participants randomized to receive a mixed meal with 25 g coconut oil
Treatment:
Dietary Supplement: Mixed meals

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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