跳至主要内容
临床试验/NCT04092972
NCT04092972Unknown不适用

Safety and Efficacy of Interventional Treatment Through Atherectomy to Improve Vascular Functions and Patency in Symptomatic Peripheral Artery Disease - Pilot Study

University Hospital, Essen1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2019年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
30
试验地点
1
主要终点
Treatment-Emerged Adverse Events

研究概览

简要总结

Interventional strategies aim to restore tissue perfusion. However, despite the simple reopening of a narrowed artery they affect endothelial function, perpetuating dysfunctional vascular homeostasis. PTA and atherectomy might alter the endothelial function but the mechanisms are incompletely understood. The primary goal of atherectomy is vessel preparation and improving compliance, which could aid in preserving vessel functions. Aim of this study is to determine safety, efficacy, patency and vessel functions in the femoropopliteal artery following atherectomy and DCB.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Peripheral artery disease, lesions in the SFA and popliteal artery.
  • •Clinical diagnosis of chronic, symptomatic lower limb ischemia as defined by Rutherford 2, 3, or 4
  • •Planed peripheral intervention TASC A-D
  • •Subject must be between 18 and 85 years old
  • •Female of childbearing potential must have a negative pregnancy test within 10 days prior to index procedure and utilize reliable birth control until completion of the 12-month angiographic evaluation
  • •Vessel diameter ≥3.0 mm and ≤7.0 mm
  • •Willing to comply with the specified follow-up evaluation
  • •Written informed consent prior to any study procedures

排除标准

  • •Thrombolysis within 72 hours prior to the index procedure
  • •Aneurysm in the femoral artery or popliteal artery
  • •Concomitant hepatic insufficiency, deep venous thrombus, coagulation disorder or receiving immunosuppressant therapy
  • •Unstable angina pectoris at the time of the enrollment
  • •Recent myocardial infarction or stroke < 30 days prior to the index procedure
  • •Life expectancy less than 12 months
  • •Septicemia at the time of enrollment
  • •Known or suspected active infection at the time of the index procedure, excluding an infection of a lower extremity wound of the target limb
  • •Known or suspected allergies or contraindications to aspirin, clopidogrel or heparin Presence of other hemodynamically significant outflow lesions in the target limb requiring a planned surgical intervention or endovascular procedure within 30 days after the index procedure

研究组 & 干预措施

Atherectomy

Experimental

Atherectomy and drug-coated balloon (DCB)

干预措施: Atherectomy (Other)

Standard care

Active Comparator

Standard care with predilation (POBA) and DCB

干预措施: POBA and DCB (Other)

结局指标

主要结局

Treatment-Emerged Adverse Events

时间窗: 6 months Follow Up

Incidence of Treatment-Emerged Adverse Events as assessed by angiography and adverse event assessment

Primary patency

时间窗: 6 months Follow Up

determined through doppler ultrasound

次要结局

  • Bail-out stent rate(6 months Follow Up)
  • Vessel stiffness(6 months Follow Up)
  • FMD local(6 months Follow Up)
  • target lesion revascularization(6 months Follow Up)
  • ABI (Ankle Brachial Index)(6 months Follow Up)
  • Systemic endothelial function(6 months Follow Up)
  • Change in Plaque burden(during baseline visit)
  • Change in plaque characteristic(during baseline visit)

研究者

发起方
University Hospital, Essen
申办方类型
Other
责任方
Principal Investigator
主要研究者

Fadi Al-Rashid

MD, Principal Investigator

University Hospital, Essen

研究点 (1)

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