The goal of this study is to evaluate the safety and effectiveness of the ePATH system in the creation of an endovascular AVF (endoAVF) in patients who require or will soon require hemodialysis and are eligible for a fistula.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Enrollment
20
An endoAVF will be created in subjects that need fistulas for hemodialysis
Sanatorio Italiano
Asunción, Paraguay
Primary Safety Endpoint
Proportion of patients that experience one or more serious ePATH device-related or ePATH portion of the procedure-related adverse events during the first 3 months following AVF creation.
Time frame: 3 months
Technical Success
Technical success: Successful creation of a fistula with the ePATH system. Verification that an endoAVF has been created with the ePATH system and that it remains patent 1-7 days after the index procedure. Patency will be defined by an experienced examiner as the presence of a bruit as detected by stethoscope, or the presence of a thrill, or with duplex ultrasonography for all study endpoints.
Time frame: 7 days
AVF maturation
Defined as an AVF that is free from stenosis or thrombosis with an arterial inflow of at least 500 ml/min and/or a diameter of at least 4 mm (as measured by duplex ultrasonography) or the patient was successfully dialysed with 2 needles.
Time frame: 3 months
Time to fistula maturation
Number of days between the index procedure and the date at which AVF maturation is achieved
Time frame: 3 months
Rate of other device or other procedure-related adverse events
Rate of serious other device (not ePATH device) or other procedure-related (not ePATH portion of the procedure) adverse events at 3 months following the index procedure
Time frame: 3 months
Rate of device and/or procedure related infections
Rate of device and/or procedure related infections at 3 months following the index procedure
Time frame: 3 months
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