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Low-density Lipoprotein Cholesterol Reduction With State-of-the-art Therapy in Secondary Prevention and Major Cardiovascular Adverse Events: Republic of Srpska Registry (RS-ACS)

U

University Clinical Centre of Republic of Srpska

Status

Unknown

Conditions

Dyslipidemias
Acute Coronary Syndrome

Treatments

Drug: Statin

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Recent trials have demonstrated that a reduction in low-density lipoprotein cholesterol (LDL-C) reduces cardiovascular adverse events following acute coronary syndrome (ACS). However, the data coming from the real-world setting are limited. Therefore, the aim of the study is to assess the association between LDL-C changes with prognosis in patients who survive ACS.

Patients with ACS will be followed for mortality and major events for at least 1 year. Changes in LDL-C between the ACS and a 6- to 10-week follow-up visit will be analysed. The associations between quartiles of LDL-C change and therapy intensity with outcomes will be investigated using adjusted Cox regression analyses.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • acute coronary syndrome

Exclusion criteria

Trial design

500 participants in 3 patient groups

High-intensity statin
Treatment:
Drug: Statin
High-intensity statin plus ezetimib
Treatment:
Drug: Statin
High-intensity statin plus ezetimib plus PCSK9 inhibitor
Treatment:
Drug: Statin

Trial contacts and locations

1

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Central trial contact

Bojan M Stanetic, MD, PhD; Tamara S Kovacevic-Preradovic, MD, PhD

Data sourced from clinicaltrials.gov

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