跳至主要内容
临床试验/NCT03975946
NCT03975946招募中不适用

Efficacy and Tolerance of RHEOpheresis in the Treatment of Peripheral Artery Disease in Hemodialysis Patients: a Prospective Randomized Single-blind Trial

Assistance Publique Hopitaux De Marseille2 个研究点 分布在 1 个国家目标入组 260 人开始时间: 2021年1月14日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
260
试验地点
2
主要终点
Percentage of absence of major amputation.

研究概览

简要总结

Peripheral arterial disease (PAD) with limb-threatening ischemia (PAD-LTI) involves both macrocirculation and microcirculation. Macrocirculatory abnormalities are accessible to revascularization techniques (endovascular or surgical) contrary to microcirculatory abnormalities. Conservative treatments have limited efficacy in patients with end-stage renal disease (ESRD). There is no alternative treatment for patients with PAD-LTI in hemodialysis.

Rheopheresis is an apheresis technique specifically designed for the treatment of microcirculatory disorders in which anomalies of rheology are at the center of physiopathology. This double cascade plasma filtration technique reduces plasma viscosity and eliminates inflammation mediators which play an essential role in PAD. This technique has already shown its effectiveness in a randomized trial in dry Age-related macular degeneration (AMD), another pathology of microcirculation. The effectiveness of rheopheresis in PAD-LTI has only been reported in a small number of cases.

This Hypothesis is that the treatment of microcirculation by rheopheresis would improve wound healing of the ischemic lesion and/or reduce major amputation and thus the prognosis of the affected limb of the patient with PAD-LTI in hemodialysis. This objective is to demonstrate the efficacy of rheopheresis, (twelve sessions), to avoid major amputation and reaches complete wound healing of ischemic lesion in the dialysis patient population with PAD-LTI. This study is prospective, Controlled, Parallel, Randomized, Single blind and Multicentric in France (12 French centers).

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
Single (Investigator)

盲法说明

The efficacy will be assessed by a vascular surgeon blinded to the study group during consultation

入排标准

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

入选标准

  • Age 18 years or more
  • End stage renal disease (ESRD) treated by hemodialysis or hemodiafiltration
  • PAD-LTI with tissue loss and/or wounds (ulcers or gangrene) with at least one of the following criterion: arterial pressure assessment at the ankle <70 millimeter of mercury (mmHg), or toe pressure 30 mmHg, or transcutaneous oximetry measurements < 40 mmHg
  • Interventional or surgical revascularization either not technically possible or no necessary. Or if revascularization has already been performed and the diagnosis of chronic critical ischemia is maintained.
  • Female of childbearing potential, will have to use highly effective methods of contraception from study start to the end.
  • Medical insurance
  • Signed informed consent

排除标准

  • Need for revascularization either endovascular (angioplasty) or surgery (bypass) of the ischemic lesion area
  • Pregnancy or breastfeeding and all the other categories of people with special protection according to the French Code de la Santé Publique (CSP): patients under legal supervision, patients hospitalized without contentment, patients admitted in social or sanitary structures for care and not research, and patients in emergency situations
  • Uncontrolled infection (persistence of fever despite appropriate antibiotic therapy)
  • Life expectancy greater than 1 year
  • Severe cognitive or psychiatric disorders
  • History of allergic reaction to dialysis membrane
  • Patients unable to give an informed consent or unwilling to participate in the study

结局指标

主要结局

Percentage of absence of major amputation.

时间窗: 8 months

Major amputation will be defined as above-the-knee amputation (AKAs) and below-the-knee amputation above the ankle (BKAs)

Percentage of complete wound healing of the ischemic lesions

时间窗: 8 months

Complete wound healing will be assessed clinically by complete epithelialization of the ischemic lesion

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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