跳至主要内容
临床试验/NCT00676494
NCT00676494已完成不适用

A Prospective, Single Arm, Multi-Center Study to Assess Performance of the Pathway PV Atherectomy System During Percutaneous Peripheral Vascular (PV) Interventions

Pathway Medical Technologies Inc.0 个研究点目标入组 172 人开始时间: 2006年2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
入组人数
172
主要终点
Major Adverse Events (MAEs) Within 30 Days

研究概览

简要总结

The Pathway PV Atherectomy System is a rotating, aspirating, expandable catheter for active removal of atherosclerotic debris and thrombus in peripheral vasculature.

This is a prospective, single arm, multi-center study to obtain safety and performance data for the Pathway PV Atherectomy System when used as a primary or adjunctive therapy for percutaneous intervention to remove atherosclerotic disease, debris, and thrombus from the lower limb peripheral vasculature.

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

  • Documented symptomatic atherosclerotic peripheral vascular disease
  • Target lesion(s) is/are located in a superficial femoral, popliteal and/or infrapopliteal arteries
  • The patient has been informed of the nature of the study and has provided informed consent
  • The patient agrees and has capability to meet study requirements and be present at the follow-up clinic visits

排除标准

  • Target lesion is located in the iliac artery.
  • Target lesion stenosis is < 70%.
  • Interventional treatment is intended for in-stent restenosis at the peripheral vascular site.
  • Patient is unable to participate for the duration of the study.
  • Patient is currently participating or has participated in a study with another investigational medical device or medication.

结局指标

主要结局

Major Adverse Events (MAEs) Within 30 Days

时间窗: 30 days

Major adverse events (MAEs) are any death, target vessel revascularization (TVR), target lesion revascularization (TLR), myocardial infarction (MI), or amputation of the treated limb that occurred within 30 days of the index procedure.

次要结局

  • Average Rutherford Classification Score at 6 Months(6 months)
  • Average Ankle Brachial Index (ABI) at 6 Months(6 months)
  • Freedom From Target Lesion Revascularization (TLR) at 6 Months(6 months)

研究者

发起方
Pathway Medical Technologies Inc.
申办方类型
Industry

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