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Study identifier: NCT03449784 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Assessment of Compliance With European and French Guidelines for the Management of Dyslipidaemias

Condition: Patient With Dyslipidemia  ·  Sponsor: University Hospital, Montpellier

PhaseN/A
Planned participants977
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Cardiovascular disease (CVD) due to atherosclerosis of the arterial vessel wall and to thrombosis is the foremost cause of premature mortality and of disability-adjusted life years in Europe, and is also increasingly common in developing countries. In the European Union, the economic cost of CVD represents annually €192 billion in direct and indirect healthcare costs. The main clinical entities are coronary artery disease (CAD), ischaemic stroke, and peripheral arterial disease (PAD). The causes of these CVDs are multifactorial. Some of these factors relate to lifestyles, such as tobacco smoking, lack of physical activity, and dietary habits, and are thus modifiable. Other risk factors are also modifiable, such as elevated blood pressure, type 2 diabetes, and dyslipidaemias, or non-modifiable, such as age and male gender. LDL-cholesterol (LDL-C) is one of the major risk factors for CVD, through its role in the development of atherosclerosis. The efficacy of statins has been demonstrated by a considerable amount of literature not only in lowering LDL cholesterol levels but also in reducing cardiovascular events, both in diabetes and non-diabetes patients. Guidelines for the management of dyslipidemia have emerged from different countries. Thereby, in 2016 the French Society of Endocrinology (SFE) and the New French Society of Atherosclerosis (NSFA) published a consensus statement on the management of dyslipidemias integrating features from European recommendations and in 2017 …

This description comes directly from the study's public registry record.

Talk to the study team

Cyril BREUKER, PharmD,Phd  ·  467337121  ·  c-breuker@chu-montpellier.fr

Always discuss trial participation with your own doctor first.

Locations (1)

UhmontpellierMontpellier, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT03449784