Paclitaxel Coated Balloon Catheter for Inhibition of Restenosis in Femoropopliteal Arteries (PACCOCATH - FEM I)
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 87
- 试验地点
- 4
- 主要终点
- angiographic late lumen loss
研究概览
简要总结
The PACCOCATH FEM study is a randomized, double-blinded German multicenter trial on the efficacy and tolerance of a paclitaxel coated balloon catheter in prevention of restenosis after femoropopliteal angioplasty.
详细描述
Background: Treatment of patients with peripheral arterial disease (PAD) in the femoropopliteal arteries by percutaneous intervention is still limited by high rates of restenosis. The aim of the present study is to evaluate the efficacy and safety of a novel method of short time local drug delivery based on a paclitaxel-coated balloon in femoropopliteal arteries.
Methods and results: The double-blind and randomized study enrolled n=79 patients with occlusion or stenosis of femoropopliteal arteries. Inclusion criteria were clinical Rutherford stage 1-5, occlusion or hemodynamic relevant stenosis (≥ 70 % diameter) of femoropopliteal arteries and successful guiding wire recanalization. The primary endpoint was the late lumen loss after 6 months follow-up as seen in angiography. Secondary endpoints included the rate of restenosis (a binary variable), change of ankle brachial index (ABI), rutherford class and major 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
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 95 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Rutherford stage 1, 2, 3, 4 oder 5
- •Occlusion or Stenosis of Superficial femoral and/or popliteal artery
- •Successful guide wire passage of the lesion
- •Patient suitable of vascular surgery in case of complication
- •Written consent
- •Patient is willing to take part in follow up examinations within the study
排除标准
- •Acute ischemia
- •Distal run off less than one vessel
- •Pregnancy
- •Hyperthyroidism
- •Thrombocytes <100.000/mm3 or >700.000/mm3, Leucocytes <3.000/mm3
- •Life expectancy less than two years
- •Patients not willing to enter the study
结局指标
主要结局
angiographic late lumen loss
时间窗: 6 months
次要结局
- binary restenosis rate; major adverse events(18 months)
