Combined Effect of LIMICOL and Physical Activity on LDL Cholesterol and Muscle Function. (L2012-12)
Hypercholesterolemia
About this trial
This is an interventional supportive care trial for Hypercholesterolemia focused on measuring Hypercholesterolemia, LDL cholesterol
Eligibility Criteria
Inclusion Criteria: BMI between 25 and 35 kg/m² Subject has a stable weight for at least three months before the start of the study. LDL ≥ 1.50 g/L 0.9 g/L ≤ triglycerides ≤ 4.00 g/L Subject able and willing to comply with the protocol and agreeing to give his informed consent in writing; Subject affiliated with a social security scheme Exclusion Criteria: Subject having a confirmed or suspected food allergy, notably to one of the components of the study product; Subject suffering from a severe chronic condition deemed incompatible with participation in the study by the investigator Subject with glaucoma Subject with uretroprostatic disorder Subjet anxious (score >9 HAD scale) Subject with diabetes Subjet with treatment anticoagulant
Sites / Locations
- Clermont Université, Université Blaise Pascal, EA 3533, Laboratoire des Adaptations Métaboliques à l'Exercice en Conditions Physiologiques et Pathologiques (AME2P), BP 10448
- CRNH-Auvergne
- Service de médecine du sport et des explorations fonctionnelles, CHU G. Montpied
- Clinique de cardiopneumologie de DURTOL
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
LIMICOL
PLACEBO
LIMICOL : red yeast rice (with monacolin K, 2 mg), artichoke leaf extract, policosanols, French maritime Pine bark extract, Garlic extract, vitamins E, B2 and B3. 1 tablet during the 3 principal meals for 12 weeks.
dicalcium phosphate, calcium citrate, vegetable magnesium stearate, microcrystalline cellulose, Maltodextrin, Tricalcium phosphate, Beet powder, Yellow coloring shellac, Brown coloring shellac. 1 tablet during the 3 principal meals for 12 weeks.