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Study identifier: NCT07311941 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Rapid Escalation of LipiD Lowering Therapy to Reduce RecUrrent Cardiovascular Event

Condition: Hyperlipidemia · Cardio Vascular Disease  ·  Sponsor: Chinese University of Hong Kong

PhaseN/A
Planned participants1000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Guangming Tan  ·  852-35051518  ·  xjldaniel@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Prince of Wales HospitalShatin, New Terrritories, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT07311941