DRKS00024582招募中不适用
Evaluation of acute and long-term results of endovascular therapy for restenosis of the popliteal artery.
niversitäts-Herzzentrum Bad Krozingen0 个研究点目标入组 150 人开始时间: 2021年2月19日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 150
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one(—)
- 性别
- All
入选标准
- •Patients with peripheral arterial disease in clinical stage 1-4 according to Rutherford-Becker classification.
- •Re-stenosis (=70% diameter reduction) or re-occlusion of the popliteal artery, confirmed by duplex sonography and/or angiography.
- •Re-stenosis or re-occlusion of the popliteal artery must not involve the superficial femoral artery and/or the anterior tibial artery and/or the tibiofibular trunk.
- •Have at least one open, nonstenosed (=50% diameter reduction) transtibial artery on the study leg.
- •Have at least one follow-up (including duplex sonography and/ or angiography), in a period of at least 12 months after re-intervention.
排除标准
- •Patients with pAVK stage 0, 5, 6 according to Rutherford-Becker classification.
- •De novo stenosis or occlusion of the popliteal artery.
- •No relevant stenosis of the target lesion (<70% diameter reduction).
- •Ectasia or aneurysm of the popliteal artery (diameter of the target lesion >7mm)
- •Re-stenosis after previous surgical therapy.
- •Treated target lesion of popliteal artery extends to superficial femoral artery and/or anterior tibial artery and/or tibiofibular trunk.
- •Occlusion or relevant stenosis (>50% diameter reduction) of all arteries of the lower leg.
- •No follow-up examinations (including duplex sonography) of the target lesion available in a period of at least 12 months after the index procedure (lost-to-follow-up).
研究者
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