Skip to content

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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05081336
Acronym
RS-ACS
Enrollment
500
Registered
2021-10-18
Start date
2021-03-01
Completion date
2023-03-31
Last updated
2021-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome, Dyslipidemias

Brief summary

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.

Interventions

DRUGStatin

Statin +/- ezetimib +/- Alirocumab

Sponsors

University Clinical Centre of Republic of Srpska
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* acute coronary syndrome

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Major Cardiovascular Adverse Events1 yearAll-cause death, Acute Coronary Syndrom, Need for Myocardial Revascularization

Secondary

MeasureTime frame
LDL reduction1 year

Countries

Bosnia and Herzegovina

Contacts

Primary ContactBojan M Stanetic, MD, PhD
bojan.stanetic@gmail.com0038765614340
Backup ContactTamara S Kovacevic-Preradovic, MD, PhD
tamara.preradovic@medicolaser.info

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026