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The Effect of Palm Olein, Olive Oil and Lard and on Risk Markers of Cardiovascular Disease

Effects of Palm Olein Versus Olive Oil on Blood Lipids, Lipoproteins and Novel Risk Markers of Cardiovascular Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00743301
Acronym
A305
Enrollment
45
Registered
2008-08-28
Start date
2008-08-31
Completion date
2009-12-31
Last updated
2008-08-28

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

Conditions

Cardiovascular Disease, Metabolic Syndrome

Keywords

CVD, Palm olein, Olive oil, Lard, healthy men, metabolic syndrome, Risk of cardiovascular disease and metabolic syndrome

Brief summary

The aim of this study is to compare the effects of a diet rich in palm olein, a fraction of palm oil, to a diet rich in olive oil and a diet rich in Danish lard on plasma total-, LDL and HDL cholesterol as well as triacylglycerol (TAG), fasting insulin and glucose, C reactive protein and plasminogen activator inhibitor 1 in healthy men. The investigators hypothesis is that palm olein and olive oil will have the same effect on plasma total cholesterol, LDL- and HDL concentration and maybe also on the secondary outcome parameters that are related to cardiovascular disease risk. This may be caused by the differences in the sn-positioning of palmitic acid in palm olein. This difference may cause the palmitic acid in palm olein to be more prone to soap formations and excretion than palmitic acid from other sources, e.g. lard. This study is a double blinded, randomized, controlled 3 x 3 week crossover intervention study, without washout periods. The participants receive the three test foods in random order, decided by draw of lots. Blood samples are drawn in duplicate (on two following days) before and after each dietary period.

Interventions

OTHERPalm olein vs olive oil and lard

17E% from test fat is incorporated into three rolls and a piece of cake

Sponsors

University of Copenhagen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. All participants must give their informed consent in writing, after having received oral and written information about the study 2. Age: 18-65 y 3. BMI: 18.5 - 30 mg/m2 4. Men 5. Healthy (no known diseases, incl. hypertension, hypercholesterolemia, diabetes and psoriasis) 6. No use of dietary supplements or blood donations two month prior to and during the intervention

Exclusion criteria

1. Current or previously cardiovascular disease 2. Diabetes Mellitus or other severe chronic disease, including severe allergies and psoriasis 3. Hypertension 4. Known or suspected abuse of alcohol, drugs or medication 5. Own request: all participants have the right to withdraw from the intervention at any given time without explanation 6. Compliance: participants may be excluded from the intervention if they do not follow the study guidelines 7. Side effects (There are no side effects expected in this study since all test fats are commercial available and use in households world wide)

Design outcomes

Primary

MeasureTime frame
total, HDL, LDL cholesterol and triacylglycerolbefore and after each type of dietary fat

Secondary

MeasureTime frame
fasting insulin and glucose, c reactive protein and plasminogen activator inhibitor 1befoer and after each dietary test fat

Countries

Denmark

Contacts

Primary ContactMarianne Raff, PhD
mrf@life.ku.dk+4535332533
Backup ContactTine Tholstrup, PhD
tth@life.ku.dk+4535332486

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026