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Active Not Recruiting NCT05639218

Impact of Optimal Pharmacotherapy on Lipid Profile and Qualitative Features of Atherosclerotic Plaques

Conditions: Atherosclerotic Cardiovascular Disease

Sex: All
Ages: 18 Years – N/A
Enrollment: 50
Sponsor: Pauls Stradins Clinical University Hospital

Location: Latvia

Summary

Lipid accumulation, with mostly emphasized role of low-density lipoprotein cholesterol (LDL-C), is the pathogenetic cornerstone of atherosclerotic cardiovascular disease. Standard hypolipidemic therapy, based on statins and ezetimibe, does not always decrease LDL-C levels enough to achieve therapeutic goals. A novel and promising direction is inhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9) in hepatocytes, subsequently reducing LDL-C receptor degradation and increasing intracellular LDL-C uptake.Aim of this study is to evaluate the effect of optimal hypolipidemic pharmacotherapy, including PCSK9 inhibitors and inclisiran, on plasma lipid profile and qualitative features of atherosclerotic plaques in very-high cardiovascular risk patients.This study enrolls patients with an established atherosclerotic cardiovascular disease, receiving PCSK9 inhibitors or inclisiran as add-on treatment to statins in maximally tolerated dose and/or ezetimibe.Effect of hypolipidemic pharmacotherapy is evaluated by analysis of plasma lipid profile parameter changes and qualitative features of atherosclerotic plaques using Near-Infrared Spectroscopy Intravascular Ultrasound Imaging (NIRS-IVUS) method.Results of the study would be sufficient for complementing evidence regarding therapeutic strategy in very-high cardiovascular risk patients.

Eligibility Criteria

Inclusion Criteria:Very high cardiovascular risk - documented atherosclerotic cardiovascular diseaseOn maximally tolerated statin and/or ezetimibe therapy for at least 1 month LDL-C treatment target <1.4 mmol/l not achievedReceiving PCSK9 inhibitor or inclisiran as add-on treatment to maximally tolerated statin dose and/or ezetimibe in the context of optimal pharmacotherapyNIRS-IVUS performed (written informed consent for the procedure signed according to regulations in the hospital)Available blood test results - plasma lipid profilePatient agrees to participate in the study (signed informed consent)Exclusion Criteria:Not fulfilling any of inclusion criteria

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05639218). StuddyBuddy aggregates publicly available trial information.