The aim is to determine the effect of investigational products on serum LDL cholesterol.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
55
Product with active ingredient vs product without active ingredient
Placebo
Nightingale Health plc
Helsinki, Finland
Change in low-density lipoprotein (LDL) cholesterol concentration (%)
Mean relative change in serum LDL cholesterol concentration during the intervention
Time frame: 0 vs 3 weeks
LDL cholesterol concentration
Mean absolute change in serum LDL cholesterol concentration during the intervention between test and control group
Time frame: 0 vs 3 weeks
total cholesterol concentration
Changes in serum total cholesterol concentration during the intervention
Time frame: 0 vs 3 weeks
High density lipoprotein (HDL) cholesterol concentration
Changes in serum HDL cholesterol concentration during the intervention
Time frame: 0 vs 3 weeks
non-HDL cholesterol concentration
Changes in serum non-HDL cholesterol concentration during the intervention
Time frame: 0 vs 3 weeks
Total triglyceride concentration
Changes in serum triglycerides concentrations
Time frame: 0 vs 3 weeks
Nuclear magnetic resonance (NMR) blood biomarkers
Changes in specific NMR blood biomarkers
Time frame: 0 vs 3 weeks
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