Primary Hypercholesterolemia Clinical Trial
Official title:
Observational Study of Superstat® (Rosuvastatin) in Hypercholesterolemia Patients in Lebanon
This study assessed the safety and efficacy of generic Rosuvastatin in reducing plasma low density lipoprotein (LDL) cholesterol in Lebanese adult patients (18 years or older) with dyslipidemia for both primary and secondary prevention based on their total cardiovascular risk. No visits or interventions, additional to the routine clinical practice, were requested or performed.
An observational, multicenter, prospective study of Lebanese adult (18 years or older)
hypercholesterolemic patients administered generic Rosuvastatin (Superstat®).
Eligible newly diagnosed hypercholesterolemic patients took generic Rosuvastatin as
prescribed by their treating physician. Assigning patients to generic Rosuvastatin was
decided within the current practice and medical indication and was independent from the
recruitment into the study.
Patients were followedâup at the clinic as per the standard practice of care. Each patient
was followed-up for a period of 2 months.
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