Efficacy and Tolerance of RHEOpheresis in the Treatment of Peripheral Artery Disease in Hemodialysis Patients

Not Applicable

Recruiting

• Conditions: Hemodialysis
• Interventions: Procedure: Rheopheresis procedure; Biological: Blood Sample; Procedure: Shamapheresis procedure

• Registration Number: NCT03975946
• Lead Sponsor: Assistance Publique Hopitaux De Marseille

Brief Summary

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).

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-05-31
• Study First Submitted QC: 2019-06-04
• Study First Posted: 2019-06-05
• Study Start: 2021-01-14
• Status Verified: 2023-07
• Last Update Submitted: 2023-07-25
• Last Update Posted: 2023-07-27
• Primary Completion: 2024-06-12
• Study Completion: 2024-06-12

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 260

Inclusion Criteria

• 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

Exclusion Criteria

• 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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
the rheopheresis group	Rheopheresis procedure	-
the rheopheresis group	Blood Sample	-
the shamapheresis group	Blood Sample	-
the shamapheresis group	Shamapheresis procedure	-

Primary Outcome Measures

Name	Time	Method
Percentage of complete wound healing of the ischemic lesions	8 months	Complete wound healing will be assessed clinically by complete epithelialization of the ischemic lesion
Percentage of absence of major amputation.	8 months	Major amputation will be defined as above-the-knee amputation (AKAs) and below-the-knee amputation above the ankle (BKAs)

Trial Locations

Locations (1)

Assistance Publique Hôpitaux de Marseille; 🇫🇷 Marseille, France