The study is a randomised, double-blind, placebocontrolled, parallel dose-response study with four study arms. Sixty subjects will be randomly allocated to consume study products containing varying amounts of plant sterol (PS) oxidation products (POP) or placebo for 6 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
60
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Charité Research Organisation GmbH
Berlin, Germany
POP (plant sterol oxidation products) value
To estimate the change from baseline in serum POP concentration after intake of various POP doses.
Time frame: 0 to 42 days
COP (cholesterol oxidation products) value
To estimate the change from baseline in serum COP concentrations after intake of various POP doses.
Time frame: 0 to 42 days
Ratio of serum POP concentration
To estimate the ratio of serum POP concentrations vs. COP concentrations after intake of various POP doses.
Time frame: 0 to 42 days
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