跳至主要内容
临床试验/NCT00349570
NCT00349570已完成不适用

Xtract™ Aspiration Catheter Registry Study

Lumen Biomedical3 个研究点 分布在 1 个国家开始时间: 2006年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
试验地点
3
主要终点
The primary objective of the study will be to evaluate the performance of the Xtract Aspiration Catheter.

研究概览

简要总结

Intra-coronary thrombosis and thromboembolism continues to be a challenge for percutaneous coronary and other vascular interventional techniques. The Xtract™ Aspiration Catheter is a single use device designed to remove fresh, soft emboli and thrombi from the arterial system using standard catheter techniques, compatible with 6 Fr guide catheters and 0.014 guidewires. The purpose of this registry study is to validate the design and demonstrate the performance of the Xtract Aspiration Catheter as a thrombectomy catheter during percutaneous intervention of vessels in the arterial system. Subjects will be enrolled during percutaneous intervention when the Interventional Physician decides a thrombectomy catheter is needed to remove thrombus during the procedure.

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

  • Planned percutaneous intervention to a native coronary, coronary vein graft, renal artery or carotid artery lesion
  • Angiographic evidence of thrombus.

排除标准

  • 未提供

结局指标

主要结局

The primary objective of the study will be to evaluate the performance of the Xtract Aspiration Catheter.

次要结局

未报告次要终点

研究者

发起方
Lumen Biomedical
申办方类型
Industry

研究点 (3)

Loading locations...

相似试验