Condition: Hypercholesterolemia · Sponsor: Fondazione IRCCS Policlinico San Matteo di Pavia
The primary outcome is to evaluate the effect of Cynacol on the change in LDL-C levels compared to Metacol after 90 days of supplementation. The secondary outcomes are to evaluate: \- the change of TC, non-HDL cholesterol (non-HDL-C), apolipoprotein B (apoB), Tg, HDL-C levels after 90 days of supplementation with Cynacol compared to Metacol. The safety outcome is collection of the adverse events not related, related or possibly related to the study products.
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| Fondazione IRCCS Policlinico San Matteo | Pavia, Lombardy, Italy | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07295327