NL-OMON42369已完成不适用
Comparison of Supera and Absolute Pro stent systems for femoro-popliteal lesions; a feasibility study - SAP feasability study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- PAD (ABI <0.90 and/or a decline of >0.15 after exercise test), Rutherford category 2, 3 or 4
- •- Significant stenoses (* 50%) and/or occlusions in the superficial femoral artery and/or popliteal artery (P1)
- •- Eligible for endovascular treatment according to international guidelines (with the expectation of stenting after PTA)
- •- Adequate inflow (<50% stenosis) either pre-existing or successfully re-established prior to target lesion treatment without complications (e.g. embolization, thrombotic event, perforation, etc.)
- •- Age * 18
排除标准
- •- Patients with PAD Rutherford category 5 and 6
- •- Contralateral lesions that require treatment within 30 days before or after the procedure
- •- Contra-indication for anticoagulant therapy
- •- Life expectancy < 1 year
- •- Known contrast allergy
- •- Pregnancy
- •- Unable to complete a questionnaire in the home language
研究者
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