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临床试验/NCT02602145
NCT02602145终止不适用

Optimal Stent Selection for the Femoropopliteal Artery

University of Nebraska1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2014年9月2日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
5
试验地点
1
主要终点
Radius of the femoropopliteal artery lumen

研究概览

简要总结

Angioplasty and stenting for atherosclerotic occlusive disease in the arteries supplying the legs (Peripheral Arterial Disease, PAD) is the most common endovascular procedure outside of the heart, but carries the highest rate of reconstruction failure. The underlying reasons for these poor results are not completely clear, but the main arterial segment within the leg, the femoropopliteal artery, appears to be significantly different from other peripheral arteries because the Superficial Femoral Artery (SFA) and Popliteal Artery (PA) that comprise the femoropopliteal artery (FPA) segment, undergo large deformations during flexion of the limb. We propose to build mathematical models of human FPAs repaired with several frequently used PAD stents. These mathematical models would be able to assess the mechanical stress in the stented SFA and PA associated with limb flexion and predict disease recurrence for arteries with different patient and lesion characteristics. Results of model predictions will be validated in patients with PAD stents who have received these stents as part of their standard of care.

详细描述

This is an observational study of PAD patients that have already received SFA and PA stents as part of their standard of care.

The purpose of this study is to determine the effects of Peripheral Artery Disease (PAD) stenting on the femoropopliteal artery. This will be achieved through the following Specific Aims:

Aim 1. Evaluate pre-operative lower extremity CTAs of patients with PAD and determine the baseline arterial geometry and lesion characteristics.

Aim 2. Evaluate the results of intraoperative angiography and blood pressure measurements proximal and distal to the stent.

Aim 3. After stenting perform post-operative lower extremity CTA and assess the amount of in-stent restenosis and changes to the arterial geometry.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Subjects eligible for participating in this study are patients with severe PAD who have:
  • endovascular repair of their femoropopliteal artery
  • standard pre-operative contrast-enhanced thin-section CTA of the lower extremities
  • intraoperative angiograms and blood pressure measurements proximal and distal to the stent during the endovascular repair
  • no aneurysmal disease of the target femoropopliteal artery
  • no prior open or endovascular repair of the target femoropopliteal artery (patients with re-interventions are not eligible)
  • at least 2 out of 3 patent crural outflow vessels
  • life expectancy >6 months
  • no iodinated contrast allergy
  • creatinine less than 1.6 g/dL (unless on chronic dialysis, dialysis patients are eligible)
  • no orthopedic prostheses in the region of interest
  • ability to comply with 6-12-month follow-up contrast enhanced thin-section CTA

排除标准

  • no endovascular repair of the femoropopliteal artery
  • endovascular or open re-intervention in the target limb
  • no pre-operative thin-section contrast-enhanced CTA of the target limb
  • no intraoperative angiogram or blood pressure measurements proximal and distal to the stent
  • aneurysmal disease of the target femoropopliteal artery
  • less than 2 patent crural outflow vessels
  • life expectancy ≤ 6 months
  • iodinated contrast allergy
  • orthopedic prosthesis in the region of interest
  • creatinine greater than 1.6 g/dL (unless dialysis patient, chronic dialysis patients are eligible)
  • inability to comply with 6-12-month contrast-enhanced CTA follow-up requirement
  • patient belongs to vulnerable population, i.e. pregnant women, prisoners, institutionalized individuals

结局指标

主要结局

Radius of the femoropopliteal artery lumen

时间窗: 6-12 months

Radius of the femoropopliteal artery lumen will be measured using follow-up CTA to assess narrowing of the artery after stent implantation.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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