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临床试验/NCT02698358
NCT02698358Unknown不适用

Korean Multicenter Registry of EPIC Stent for Iliac Artery Disease: (K-EPIC Registry)

Yonsei University1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2015年12月最近更新:
适应症

试验速览

阶段
不适用
入组人数
68
试验地点
1
主要终点
Primary patency

研究概览

简要总结

  • Prospective, single-arm, multi-center registry study
  • A total of 150 subjects with iliac artery disease who meet all inclusion and exclusion criteria will be included.
  • Patients will be followed clinically for 12 months after the procedure.
  • Duplex ultrasound, CT or catheter-based angiography follow-up according to participating hospital's protocol will be performed at 12 months.
  • Presence of stent fracture will be evaluated by plain radiography or fluoroscopy at 12 months.
  • Quality of life by standardized questionnaires (at baseline & at 1 & 12 months)

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
19 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 19 years of older
  • Symptomatic peripheral artery disease:
  • Moderate or severe claudication (Rutherford category 2 or 3)
  • Critical limb ischemia (Rutherford category 4)
  • Iliac artery lesions with stenosis > 50%
  • Patients with signed informed consent

排除标准

  • Acute critical limb ischemia
  • Severe critical limb ischemia (Rutherford category 5 or 6)
  • Known hypersensitivity or contraindication to any of the following medications: heparin, aspirin, clopidogrel, cilostazol, or contrast agents
  • In-stent restenosis lesions (Restenosis lesions without previously implanted stents are eligible to the enrollment)
  • Bypass graft lesions
  • Age > 85 years
  • Severe hepatic dysfunction (> 3 times normal reference values)
  • Significant leucopenia, neutropenia, thrombocytopenia, anemia, or known bleeding diathesis
  • LVEF < 40% or clinically overt congestive heart failure
  • Pregnant women or women with potential childbearing
  • Life expectancy <1 year due to comorbidity
  • Untreated proximal inflow disease of aorta or the ipsilateral iliac arteries (more than 50% stenosis or occlusion)

结局指标

主要结局

Primary patency

时间窗: 12 months

Absence of restenosis \>50% based on an imaging study (Duplex ultrasound, CT angiography or catheter angiography) at 12 months

次要结局

  • Target lesion revascularization rate(12 months)
  • Stent fracture rate(12 months)
  • Quality of life by standardized questionnaires(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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