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临床试验/NCT03036241
NCT03036241已完成不适用

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

Helsinki University Central Hospital0 个研究点目标入组 39 人开始时间: 2013年1月23日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
39
主要终点
TLR

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 dialysis fistulae.

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 dialysis fistulae 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, Investigator)

入排标准

性别
All
接受健康志愿者

入选标准

  • Any dialysis access w/ native vessels warranting intervention

排除标准

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

结局指标

主要结局

TLR

时间窗: 12 months

Target lesion revascularization, ie. re-intervention to the same lesion

Occlusion of access

时间窗: 12 months

Any loss of dialysis access due to thrombosis

次要结局

  • Primary assisted patency(12 months)
  • Death(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

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