跳至主要内容
临床试验/NCT06264843
NCT06264843招募中不适用

Open, Prospective, Multicentre Study Addressing the Immediate Benefits and the Prognostic Value of Intraoperative Completion Control Following Infrainguinal Bypass Surgery in Chronic Limb-Threatening Ischemia (CLTI) Patients

Medistim ASA1 个研究点 分布在 1 个国家目标入组 450 人开始时间: 2024年11月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
Medistim ASA
入组人数
450
试验地点
1
主要终点
Primary graft patency rate

研究概览

简要总结

The goal of the study is to identify and validate flow measurement and ultrasound images in patients undergoing vein bypass surgery below-knee and above ankle

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Chronic Limb-Threatening Ischemia as defined by presence of Peripheral Artery Disease (PAD) in combination with rest pain, gangrene, or a lower limb ulceration>2 weeks duration (ref Global Guidelines)
  • •Atherosclerotic infra-popliteal PAD
  • •Adequate distal anastomotic target (crural, tibial or popliteal below the knee with one single run-off) between knee and ankle distal to the stenotic/occluded segment.
  • •Available autogenous vein conduit based on preoperative vein mapping.
  • •Understand the nature of the procedure and willingness to comply with protocol. Attend follow-up appointments and provide written informed consent.

排除标准

  • •Bypass with artificial conduit or cryopreserved allografts
  • •Bypass for non-atherosclerotic lesions
  • •Life-expectancy less than 2 years
  • •Any psychological, developmental, physical or emotional disorder that the investigator believes would interfere with surgery or follow-up.
  • •Any condition that the investigator believes should exclude participation.
  • •Excessive risk for adverse events during open surgery as judged by the investigator.

研究组 & 干预措施

Patency of lower extremity vein bypass grafts

Primary patency of lower extremity vein bypass grafts at one year

干预措施: MiraQ with Transit-Time Flow Measurement (TTFM) and L15 High Frequency Ultrasound (HFUS) probes (Device)

结局指标

主要结局

Primary graft patency rate

时间窗: at 1 year

Freedom from any repeat graft intervention, graft thrombosis, or clinically significant stenosis (\>70% by either Duplex criteria or angiographic imaging) in the bypass

次要结局

未报告次要终点

研究者

发起方
Medistim ASA
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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