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临床试验/NCT03023098
NCT03023098已完成不适用

Drug-eluting Balloon vs. Conventional Balloon in the Treatment of (re)Stenosis - a Randomized Prospective Study

Helsinki University Central Hospital2 个研究点 分布在 1 个国家目标入组 57 人开始时间: 2013年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
57
试验地点
2
主要终点
TLR (Target lesion revascularization)

研究概览

简要总结

The purpose of this study is to determine whether the use of drug-eluting balloons is effective in the treatment of (re)stenosis in bypass vein grafts.

详细描述

Drug-eluting devices have proved beneficial in the treatment of stenosis in native coronary and lower limb arteries. Stenosis and restenosis is a known problem in bypass vein grafts, and drug-eluting devices might be beneficial in this field as well.

In the procedure a conventional balloon is passed through the stenosis which is then dilated. After this patients are randomized before a second dilatation with either a conventional balloon or a drug-coated balloon.

The stenosis is evaluated preoperatively and followed up by means of ultrasound by a vascular technician. Follow-up will end at 12 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
Double (Participant, Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • Any venous bypass with stenosis warranting intervention

排除标准

  • Previous PTA with drug-eluting balloon, thrombolysis, coagulopathy

结局指标

主要结局

TLR (Target lesion revascularization)

时间窗: 12 months

Any reintervention to the same lesion.

Graft occlusion

时间窗: 0-12 months

Occlusion of the bypass graft

次要结局

  • Major amputation(0-12 months)
  • Death(0-12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Maarit Venermo

Professor of Vascular Surgery

Helsinki University Central Hospital

研究点 (2)

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