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临床试验/NCT01353651
NCT01353651已完成4 期

Endovascular Versus Open Repair of the Common Femoral Artery: a Randomized Trial (TECCO)

Nantes University Hospital18 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2011年2月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
120
试验地点
18
主要终点
Morbid-mortality rate at 30 days

研究概览

简要总结

Even though the indication for endovascular therapy has been enlarged, open repair of common femoral artery is still considered as the treatment of choice. A recent pilot study showed that endovascular repair of the CFA seems to be a safe technique of revascularization with acceptable initial results at 12 months (Azema et al, Eur J Vasc Endovasc Surg, 2011, in press). TECCO, a French randomized and controlled trial, has been set up to compare open and endovascular procedures for the treatment of CFA atherosclerotic lesions.

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
None

入排标准

年龄范围
40 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 40 and 90 years-old
  • De novo atheromatous common femoral artery stenosis
  • Symptomatic lesions (Rutherford stages 3, 4, 5 and 6)
  • Haemodynamically significant lesion
  • Written informed consent

排除标准

  • Restenosis
  • Non-atheromatous lesions (dysplasia, post-traumatic, inflammatory)
  • external iliac thrombosis and / or common femoral side to treat
  • Contraindication to open surgery or endovascular treatment
  • Contraindication to anesthesia
  • Indication of aorto-femoral, ilio-femoral, femoral-popliteal or femoro-tibialis bypass to associate with the common femoral revascularization
  • Indication of a surgical approach to the external iliac artery through a retroperitoneal
  • Asymptomatic lesions
  • Life expectancy less than one year
  • Refusing patient
  • Inability to monitor during the test period
  • Participation in another clinical trial
  • Pregnant Women
  • No written informed consent

研究组 & 干预措施

Endovascular treatment

Experimental

干预措施: Endovascular treatment using self expandable nitinol STENTS (Device)

Open repair treatment

Active Comparator

干预措施: Open repair treatment (Device)

结局指标

主要结局

Morbid-mortality rate at 30 days

时间窗: 30 days

Morbid-mortality rate is defined by: Death, general complications and local complications requiring re-admission and / or reoperation.

次要结局

  • Technical success(1 month)
  • Hospital length of stay(1 month)
  • Primary sustained clinical improvement(24 months)
  • Target lesion revascularization(24 months)
  • In-stent restenosis(24 months)
  • Stent fracture(24 months)
  • Secondary sustained clinical improvement(24 months)
  • Target extremity revascularization(24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (18)

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