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临床试验/NCT00500279
NCT00500279Unknown4 期

Effects of Celecoxib On Restenosis After Coronary Intervention and Evolution of Atherosclerosis Trial

Seoul National University Hospital2 个研究点 分布在 1 个国家目标入组 900 人开始时间: 2006年11月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
入组人数
900
试验地点
2
主要终点
late luminal loss on quantitative coronary angiography

研究概览

简要总结

To evaluate the effect of celecoxib use for 3 month after drug-eluting stent implantation

  • on restenosis
  • on clinical outcome such as target lesion revascularization, thrombotic event, myocardial infarction, death
  • on inflammatory biomarkers

详细描述

Restenosis is the major adverse effect of coronary stent implantation. Drug-eluting stent has markedly reduced restenosis as compared with bare-metal stent, but restenosis is still the main cause of repeat coronary intervention after drug-eluting stent implantation. After coronary stent implantation, inflammatory reaction occurs in vessel wall and vascular smooth muscle cells proliferate. Celecoxib is well known to have anti-proliferative effect as well as anti-inflammatory effect, and safety of this drug is well-established. Celecoxib use for 6 month after paclitaxel-eluting stent implantation significantly reduced neointimal growth and repeat intervention without increase in adverse effect. Because inflammatory reaction seems to occur in very early period after vessel injury, reduced use of celecoxib may also be effective.

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
30 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •angina pectoris or a positive stress test with native coronary artery lesions feasible for drug-eluting stent implantation

排除标准

  • •acute or recent ST segment elevation myocardial infarction (within four weeks)
  • •left main coronary artery disease
  • •hepatic dysfunction (AST or ALT > 120 IU/L )
  • •renal dysfunction (serum creatinine > 2.0 mg/dl)
  • •severe congestive heart failure (NYHA class > 2)
  • •left ventricular ejection fraction < 30%
  • •hemodynamically unstable condition
  • •definite intracoronary thrombus
  • •contraindication or history of allergy to aspirin, clopidogrel, or celecoxib
  • •warfarin use
  • •expected survival less than two years due to other medical conditions
  • •patients already taking any COX-3 inhibitor or NASIDS

结局指标

主要结局

late luminal loss on quantitative coronary angiography

时间窗: six month

次要结局

  • target lesion revascularization, myocardial infarction, death, thrombotic events(six and eighteen month)

研究者

申办方类型
Other

研究点 (2)

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