The WRAP Study aims to expand and understand the safety and efficacy data on the WRAPSODY Endoprosthesis System in a real-world population.
Prospective, multicenter, observational study to evaluate the Merit WRAPSODY™ Endoprosthesis for treatment of stenosis or occlusion within the dialysis outflow circuit of an arteriovenous (AV) fistula or AV graft (The WRAP Registry)
Study Type
OBSERVATIONAL
Enrollment
500
Target Lesion Primary Patency (TLPP)
Proportion of subjects with Target Lesion Primary Patency (TLPP) (Primary Effectiveness Endpoint)
Proportion of subjects with Target Lesion Primary Patency (TLPP) at 6 Months. TLPP is defined as freedom from clinically-driven target lesion revascularization (CD-TLR) or target lesion thrombosis measured through 6 months post-procedure, which is the time interval of uninterrupted patency after study procedure to the next intervention performed on the target lesion or uncorrectable target lesion occlusion.
Time frame: 6 months
Proportion of subjects without any localized or systemic safety events (Primary Safety Endpoint)
Proportion of subjects without any localized or systemic safety events through 30 days post-index procedure that affect the access or venous outflow circuit and resulted in reintervention, hospitalization, or death (not including stenosis or thrombosis).
Time frame: 30 days
Proportion of subjects with Target Lesion Primary Patency
Proportion of subjects with Target Lesion Primary Patency
Time frame: 12 and 24 months
Proportion of subjects with Assisted Target Lesion Primary Patency (aTLPP)
Proportion of subjects with Assisted Target Lesion Primary Patency (aTLPP)
Time frame: 6, 12 and 24 months
Proportion of subjects with Access Circuit Primary Patency (ACPP)
Proportion of subjects with Access Circuit Primary Patency (ACPP)
Time frame: 6, 12 and 24 months
Rates of procedure- and device-related adverse events
Rates of procedure- and device-related adverse events
Time frame: Index procedure, 30 days, and months 6
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