跳至主要内容
临床试验/NCT02750605
NCT02750605已完成不适用

Randomized Trial Comparing Drug Coated Balloon vs Plain Balloon Angioplasty in Critical Limb Ischemia and Treatment of Long Lesions in Crural Arteries

Skane University Hospital2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2016年2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
70
试验地点
2
主要终点
Clinical driven target lesion revascularization (TLR)

研究概览

简要总结

The purpose of this trial is to compare short- medium long-term results in treatment of PAD (peripheral arterial disease) in the crural arteries with either drug coated balloon or conventional balloons in a prospective , randomized, single center study

Results will be defined as:

Limb salvage, Event-free survival, Freedom from TLR (target lesion revascularization), Primary patency, Clinical success, Serious adverse events, and the patients will be followed-up for 1 years.

Primary endpoints:

Primary Patency at 12 months, TLR (clinical driven),

Secondary endpoints:

Event free survival, Clinical success at 6,12 months, Technical success, Serious adverse events,

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
Single (Participant)

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

  • Critical limb ischemia. Rutherford class 4-6
  • Crural disease, long lesions, more than 2 cm.
  • Life expectancy > 1year
  • > 18 years

排除标准

  • Pregnancy
  • Patients disapproval
  • Allergy to drug or contrast

结局指标

主要结局

Clinical driven target lesion revascularization (TLR)

时间窗: 12 months

Porportion of patients that needs retreatment in in the monitored arterial segment

Primary patency of treated crural vessels

时间窗: 12 months

Evaluation with MRA (Magnetic Resonans Angiography) at 12 months, regarding binary restenosis or occlusion in the treated arterial segment. Proportion of treated segments that remains open.

次要结局

未报告次要终点

研究者

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

Torbjorn Fransson

Consultant, Vascular Surgery

Skane University Hospital

研究点 (2)

Loading locations...

相似试验