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临床试验/NCT04594889
NCT04594889Unknown不适用

Comparison of Sirolimus vs Paclitaxel Drug Eluting Balloon for Below-the-knee Angioplasty in Critical Limb Ischemia

Ospedale San Donato2 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2020年10月14日最近更新:
适应症

试验速览

阶段
不适用
入组人数
170
试验地点
2
主要终点
Late Luminal Loss (LLL)

研究概览

简要总结

The objective of this study is to compare the remote patency of paclitaxel versus sirolimus eluting balloons in patients with CLI undergoing tibial artery revascularization. Patients will be randomized 1:1 to Paclitaxel eluting balloon (Litos, ACOTEC ltd) or sirolimus eluting balloon (Magic touch, Concept Medical) after optimal balloon angioplasty. The primary endpoint of the study is the late luminal loss at 6 months angiography. Secondary endpoint are major amputation, clinically driven target lesion revascularization and vessel reocclusion (duplex) at 12 months.

详细描述

Critical ischemia of the limb is considered one of the most severe clinical scenario of atherosclerotic disease involving the lower limb because it is associated with a high degree of mortality and morbidity. Below the knee arterial disease is the basis of critical limb ischemia (CLI). It is generally characterized by the involvement of multiple tibial arteries, long lesions and high rate of hronic total occlusions. Percutaneous treatment of tibial arteriopathy is characterized by high restenosis (70%). The advent of the drug-eluting strategy has led to a reduction in the restenosis of the femoral and tibial district with paclitaxel eluting devices. Data are not yet available on sirolimus eluting devices, both for the femoropopliteal and tibial districts. The objective of this study is to compare the remote patency of paclitaxel (Lithos) vs. the sirolimus (magic touch) eluting balloons in patients with CLI undergoing tibial artery revascularization.

The study will enroll only patients with optimal balloon angioplasty defined by angiographic and ultrasound criteria in order to avoid biases related to potentially unbalanced suboptimal angioplasty results in both groups. The patients will be followed by either interventionalists as well as diabetic foot specialists in order to optimize their surveillance for lesion healings and vessel patency and reduced dropout.

Participating

Centers Cardiovascular disease department (San Donato Hospital, Arezzo, Italy) O.U. Cardiology (San Iacopo Hospital, Pistoia, Italy) O.U. Cardiology (San Giuseppe Hospital, Empoli, Italy) O.U Hemodynamics (A.O.U.C. Careggi, FlorenCe, Italy)

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
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • Age between 18 and 85 years
  • CLI Rutherford class 4-
  • Stenosis or occlusion with length >= 4 cm involving a tibial artery
  • Presence of angiographic distal runoff to the foot (stage 1-2a-2b of the Kawarada classification)
  • Presence of optimal angioplasty result defined as residual stenosis < 50%, absence of flow limiting dissection, absence of vessel perforation, absence of distal embolization by angiography and biphasic or triphasic flow at ultrasoud evaluation of the target vessel

排除标准

  • Known allergy to one of the drugs in the study
  • Contraindications to antiplatelet therapy
  • Life expectancy less than 1 year
  • Major amputation planned before angiography
  • Inability to obtain informed consent -

结局指标

主要结局

Late Luminal Loss (LLL)

时间窗: 6 months

LLL will be measured in the treated segment obtained subtracting the minimal lumen diameter at 6-month angiographic follow.up with minimal lumen diameter post intervention

次要结局

  • Target vessel occlusion (TVO)(12 months)
  • Clinically driven target lesion revascularization(12 months)
  • Major limb amputation(12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Francesco Liistro

Cardiovascular Intervention Director

Ospedale San Donato

研究点 (2)

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