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临床试验/NCT06520904
NCT06520904招募中4 期

Effect of PCSK9 Inhibitors on Coronary Atherosclerotic Plaques Derived From Optical Coherence Tomography in Patients With Premature Coronary Artery Disease: a Randomized Controlled Trial

First Affiliated Hospital of Xinjiang Medical University1 个研究点 分布在 1 个国家目标入组 396 人开始时间: 2024年7月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
396
试验地点
1
主要终点
Calcification

研究概览

简要总结

The presence of coronary atherosclerotic vulnerable plaque significantly impacts the clinical outcomes of patients diagnosed with coronary artery disease (CAD). However, the influence of PCSK9 inhibitors on stabilizing coronary atherosclerotic plaques in individuals with early-onset CAD, evaluated through optical coherence tomography (OCT), remains inadequately understood. Moreover, there is a notable absence of relevant randomized controlled trials investigating this phenomenon. This current study represents a single-center, randomized, controlled, open-label trial conducted among Asian patients with early-onset CAD. Its principal objective was to explore the effects of PCSK9 inhibitors on coronary atherosclerotic plaque morphology as assessed by OCT.

详细描述

Following initial percutaneous coronary intervention (PCI) for culprit lesions in patients with early-onset coronary artery disease (CAD) and ≥2 additional lesions meeting baseline lipid criteria, optical coherence tomography (OCT) was employed to evaluate non-culprit lesion sites for detailed characterization of plaque features including calcification, fibrosis, fibrolipid deposition, necrosis, minimum fibrous cap thickness (mFCT), and maximum lipid arc (MLA). Subsequently, patients were randomized in a 1:1 ratio to receive either intensive statin therapy alone or a combination of PCSK9 inhibitor with moderate-intensity statin therapy, using a random number allocation method. After 1 year of treatment and follow-up, OCT reassessment of non-culprit vessel critical lesions was conducted, documenting plaque characteristics such as calcification, fibrosis, fibrolipid content, necrosis, as well as stability parameters like mFCT and MLA at lesion sites. OCT findings were compared longitudinally within each treatment group and between groups receiving PCSK9 inhibitor combined with statin therapy versus intensive statin therapy alone. Baseline clinical profiles, biochemical markers, imaging findings, and incidence of adverse cardiovascular events during the follow-up period were also meticulously recorded for all enrolled early-onset CAD patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men aged 18-55 years and women aged 18-65 years;
  • CAD patients with coronary angiographically confirmed lesions in ≥2 vessels; at least one vessel was critically diseased (50-70% stenosis level);
  • LDL-C >3.4 mmol/L without regular statin therapy or LDL-C >1.8 mmol/L after 4 weeks of statin lipid-lowering therapy.

排除标准

  • Known allergies or contraindications to PCSK9 inhibitors and/or statin therapy;
  • Prior use of PCSK9 inhibitors;
  • Prior history of hemorrhagic stroke;
  • Prior coronary artery bypass grafting or coronary intervention;
  • Inability to perform OCT imaging or unclear imaging;
  • Severe renal insufficiency (creatinine clearance < 30 mL/min);
  • Severe hepatic dysfunction;
  • Baseline triglycerides > 5.6 mmol/L;
  • Pregnant or lactating women;
  • Life expectancy not exceeding 1 year;
  • In the judgment of the investigator, unsuitable for this study for any reason.

研究组 & 干预措施

PCSK9 inhibitor group

Experimental

PCSK9 Inhibitors Combined with Moderate-Intensity Statin Therapy

干预措施: PCSK9 inhibitor (Drug)

Intensive statin group

Other

Intensive statin therapy

干预措施: Statin (Drug)

结局指标

主要结局

Calcification

时间窗: Immediate and 1 year after PCI

calcification

Fibrosis

时间窗: Immediate and 1 year after PCI

fibrosis

Fibrolipid deposition

时间窗: Immediate and 1 year after PCI

fibrolipid deposition

Necrosis

时间窗: Immediate and 1 year after PCI

necrosis

MLA

时间窗: Immediate and 1 year after PCI

maximum lipid arc

mFCT

时间窗: Immediate and 1 year after PCI

minimum fibrous cap thickness

次要结局

未报告次要终点

研究者

发起方
First Affiliated Hospital of Xinjiang Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhenyan Fu, PHD

Principle Investigator

First Affiliated Hospital of Xinjiang Medical University

研究点 (1)

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