Clinical Trial

Rapid Escalation of LipiD Lowering Therapy to Reduce RecUrrent Cardiovascular Event

Study acronym: REDUCE-Lipid
Recruiting
View on ClinicalTrials.gov →
Summary
Hyperlipidaemia especially elevation of low-density lipoprotein cholesterol (LDL-C) is known to be the main contributor to the development of atherosclerotic cardiovascular disease (ASCVD). Lowering LDL-C have been shown to reduce the risk of ASCVD2,3. Both the American Heart Association (AHA) and the European Society of Cardiology (ESC) advocated aggressive LDL-C target with statin being the first-line lipid-lowering therapy (LLT). However, a significant portion of patients did not attain their LDL-C goal in our locality. Statin no adherence, low uptake of adjuvant non-statin LLT, and therapeutic inertia are few potential causes for not achieving the LDL-C target. ESC recommends repeating blood test in 6-8 weeks after addition or alternation of LLT, but this recommendation was not routinely followed in current local practice due to resources constrain. This registry therefore aims to investigate the strategy of frequent monitoring of LDL-C and titration of LLT in achieving LDL-C treatment target at a dedicated specialist clinic.
Trial Details
NCT Number NCT07311941
Lead Sponsor Chinese University of Hong Kong
Conditions Hyperlipidemia, Cardio Vascular Disease
Enrollment 1,000 participants
Start Date 2024-12-30
Primary Completion 2030-12-31 (estimated)
Study Completion 2031-06-30 (estimated)
Updated on ClinicalTrials.gov 2025-12-31