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临床试验/NCT00233792
NCT00233792已完成1 期

An Evaluation of the Sirolimus Coated Modified BX VELOCITY Balloon-Expandable Stent in the Treatment of Patients With de Novo or Restenotic Native Coronary Artery Lesions.

Cordis Corporation2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 1999年12月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
30
试验地点
2
主要终点
Assessment of in-stent percent diameter stenosis (%DS) measured by quantitative coronary angiography.

研究概览

简要总结

This is a single center, non-randomized study. Patients will be treated with the sirolimus coated Bx VELOCITY Balloon-Expandable Stent mounted on the Raptor OTW SDS. Patients will have a repeat angiography at four months and will be followed for twelve months post-procedure.

详细描述

This is a single center, non-randomized study of the Bx VELOCITY Balloon-Expandable Stent coated with sirolimus (140µg/cm2) and formulated for fast or slow release. The sirolimus coated stent is mounted on the Raptor OTW SDS. Approximately 30 patients with de novo or restenotic native coronary artery lesions <=18mm in length and >=3.0 to >=3.5 mm in diameter by visual estimate who meet all eligibility criteria will be treated with the sirolimus coated Bx VELOCITY stent(s). Patients will be followed for five years post-procedure and will have a repeat angiography at 4 months, 12 months, 24 months, and 48 months.

研究设计

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

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

  • Diagnosis of angina pectoris as defined by Canadian Cardiovascular Society Classification (CCS) or a positive ischemia study;
  • Single de novo or restenotic lesion requiring treatment in a major native coronary artery;
  • Target lesion is <=18mm in length (visual estimate);
  • Target lesion is >=3.0mm and <=3.5mm in diameter (visual estimate);
  • Target lesion stenosis is >50% and <100% (visual estimate);

排除标准

  • A Q-wave or non-Q-wave myocardial infarction within the preceding 72 hours unless the CK and CK-MB enzymes are back to normal;
  • Unprotected left main coronary disease with >=50% stenosis;
  • Have an ostial target lesion;
  • Angiographic evidence of thrombus within target lesion;
  • Calcified lesions which cannot be successfully predilated;
  • Ejection fraction <=30%;
  • Target lesion involves bifurcation (either stenosis of both main vessel and major branch or stenosis of just major branch);
  • Totally occluded vessel;

结局指标

主要结局

Assessment of in-stent percent diameter stenosis (%DS) measured by quantitative coronary angiography.

时间窗: post procedure and 6 months

次要结局

  • Target vessel failure (TVF).(6 months)
  • Assessment of lesion morphology by intravascular ultrasound (IVUS).(post procedure and 6 months)

研究者

申办方类型
Industry

研究点 (2)

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