跳至主要内容
临床试验/NCT00232830
NCT00232830已完成3 期

Trial to Assess the Use of the Cypher TM Stent in Acute Myocardial Infarction Treated With Balloon Angioplasty

Cordis Corporation2 个研究点 分布在 2 个国家目标入组 715 人开始时间: 2003年10月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
715
试验地点
2
主要终点
Composite of target vessel failure (TVF) defined as target vessel revascularization, recurrent myocardial infarction, or cardiac death that could not be clearly attributed to a vessel other than the target vesselpost-procedure.

研究概览

简要总结

The main objective of this study is to assess the effectiveness and safety of the CYPHER™ (CYPHER SELECT™) (Sirolimus-eluting) stent in reducing the occurrence of a composite endpoint of target vessel failure (TVF) in subjects treated for acute myocardial infarction as compared to a bare metal stent.

详细描述

This is an international, multicenter (up to 52 sites), randomized, single-blind study in patients with an acute myocardial infarction treated with the CYPHER™ (Sirolimus-eluting) stent as compared to the bare stents.

Patients with de novo native coronary artery lesions will be treated with the CYPHER™ (Sirolimus-eluting) stent or a bare stent. Subjects will be followed at 30 days, 6 months and at 1, 3, 4 and 5 years post-procedure. 200 subjects will have an angiographic follow-up at 8 months.

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
Single (Participant)

入排标准

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

入选标准

  • •Have prolonged, continuous (lasting at least 20 minutes) chest pain despite administration of nitrates and onset within 12 hours of randomization, and one of the following:
  • •ST segment elevation >=1mm in standard leads and >=2mm in 2 or more contiguous precordial leads with reciprocal ST depression
  • •New or presumably new left bundle branch block (LBBB)
  • •The culprit lesion must be identified on a de novo native coronary artery and an emergency angioplasty must be possible. The culprit site must be visualized before the stent implantation;

排除标准

  • •Killip class > 2 upon arrival to the cath-lab;
  • •Significant (>50%) stenosis proximal or distal to the target lesion that might require revascularization or impede inflow or runoff;
  • •Evidence of massive thrombus in the infarct related artery distally to the culprit lesion;
  • •Documented left ventricular ejection fraction <=30%;
  • •Target lesion is located in an arterial or venous by-pass graft;
  • •ECG documented evidence of prior myocardial infarction;
  • •Patient who received thrombolytic therapy for the current AMI before enrollment in this study.

研究组 & 干预措施

1

Experimental

Cypher Sirolimus-eluting Coronary Stent

干预措施: drug-eluting stent (Device)

2

Active Comparator

Bare-metal stent

干预措施: bare-metal stent (Device)

结局指标

主要结局

Composite of target vessel failure (TVF) defined as target vessel revascularization, recurrent myocardial infarction, or cardiac death that could not be clearly attributed to a vessel other than the target vesselpost-procedure.

时间窗: 1 and 6 months and at 1, 3, 4, and 5 years post-procedure.

次要结局

  • recurrence of myocardial infarction(1, 3, 4 and 5 years post-procedure)
  • revascularization of the target vessel (TVR)(1, 3, 4 and 5 years post-procedure)
  • recurrence of ischemia(1, 3, 4 and 5 years post-procedure)
  • cardiac death(1, 3, 4 and 5 years post-procedure)

研究者

申办方类型
Industry

研究点 (2)

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