About this trial

The pharmacological reduction of LDL-C lowers cardiovascular risk and is therefore a priority in cardiovascular secondary prevention. The achievement of LDL-C target levels in Germany, Europe, and worldwide is inadequate, despite a wide array of lipid-lowering medications. Only a small proportion of post-myocardial infarction patients reach their LDL-C target range within a year. There is a significant need for new strategies to improve LDL-C target achievement and thereby reduce the occurrence of secondary cardiovascular events.

The aim of the study is to establish a basis for improving prevention by achieving the target LDL level effectively and quickly in patients with high and very high cardiovascular risk profiles.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Patients with acute coronary syndrome in the last 6 months and not having reached the LDL target value

Signed informed consent

Disqualifiers

Persons unable to understand the study

Persons unable or unwilling to perform self-measurements

Persons unable or unwilling to undergo additional cholesterol-lowering therapy to reach the LDL target

Pre-menopausal women without contraception

Trial design

Treatments tested in this trial

  • Cholesterol self-measurement

Treatment groups

200 Participants
are divided into 2 treatment groups

Locations

1
Clinic of cardiology University clinic Leipzig04103, LeipzigSaxony, Germany

Sponsors and collaborators

University of Leipzig

Lead sponsor