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临床试验/NCT07197242
NCT07197242尚未招募不适用

Assessment of Lipoprotein(a) in Patients Undergoing Elective Percutaneous Coronary Revascularization: Implications for Cardiovascular Risk Stratification

Assiut University0 个研究点目标入组 156 人开始时间: 2026年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
156
主要终点
Incidence of major adverse cardiovascular events (MACE)

研究概览

简要总结

The study investigates the role of Lipoprotein(a) [Lp(a)] levels in predicting cardiovascular risk and adverse events in patients undergoing elective percutaneous coronary intervention (PCI).

详细描述

his is a multicenter prospective observational cohort study conducted at Assiut University Heart Hospital and affiliated centers. The study focuses on patients undergoing elective (non-ACS) PCI for stable coronary artery disease. Baseline Lp(a) levels will be measured pre-PCI using isoform-insensitive immunoassays, and patients will be followed for 24 months to document cardiovascular outcomes. The primary goal is to assess whether elevated Lp(a) (≥125 nmol/L) independently predicts 2-year major adverse cardiovascular events (MACE) beyond conventional risk factors and procedural complexity. The study also aims to evaluate the prevalence of elevated Lp(a) among this population and its incremental prognostic value for refining risk stratification models such as SYNTAX II/ACEF. Collected blood samples will be stored in a biobank for future exploratory analyses.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Adults aged 18 years or older
  • Undergoing elective PCI for stable coronary artery disease
  • Ability to provide informed consent
  • Willingness to undergo blood sampling prior to PCI

排除标准

  • Acute coronary syndrome within 30 days
  • Cardiogenic shock
  • Prior heart transplant or left ventricular assist device (LVAD)
  • Life expectancy less than 1 year due to non-cardiac causes
  • Participation in a blinded Lp(a)-lowering outcome trial at the time of enrollment

结局指标

主要结局

Incidence of major adverse cardiovascular events (MACE)

时间窗: one year

Incidence of all non-fatal myocardial infarction, and ischemia-driven target vessel revascularization or or definite/probable stent thrombosis.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

ahmed gamal abdelhakeem ahmed

resident at Cardiology Department

Assiut University

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