Arteriovenous Fistula (AVF) is a surgically created circuit used for hemodialysis in patient with End Stage Renal Disease (ESRD). A functioning dialysis vascular access is critical to the delivery of life-saving hemodialysis (HD) treatment for these patients. Unfortunately, neointimal hyperplasia frequently occurs within the dialysis vascular access, resulting in stenosis, poor flow and thrombosis with loss of function. The cephalic vein forms the outflow conduit for radiocephalic (RC) and brachiocephalic (BC) AVF. At the perpendicular portion of the cephalic vein, the cephalic arch is often prone to developing hemodynamically significant stenosis. The prevalence of cephalic arch stenosis is reported to be 39% in brachiocepahlic and 2% in radiocephalic AVF. The current gold standard therapy for treatment of AVF stenosis is plain balloon angioplasty (BA). Paclitaxel coated balloon (PCB) angioplasty has also been shown recently to be superior to plain BA in the treatment of stenosis in dialysis vascular access. By releasing paclitaxel, which is an anti-proliferation drug, locally into the vessel wall during balloon contact, it will blunt the acceleration of intimal hyperplasia response, resulting in improved primary patency after angioplasty. The use of stent grafts for recurrent CAS has been demonstrated to increase patency of AVF compared to BA and bare stents. However, stent grafts are prone to edge restenosis that tend to occur within 5mm of each end of SG due to neointimal hyperplasia from the end of the stent migrating towards the center. We postulate that stent graft with PCB angioplasty of the stent edge is more effective than PCB alone in maintaining the patency of AVF with cephalic arch stenosis. Therefore, we aim to perform a randomized controlled trial to compare the 6-month unassisted patency rate of treatment of recurrent CAS with stent graft and PCB angioplasty of both stent edge versus PCB alone.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
80
CAS treated with PCB only
CAS treated with PCB first before deployment of stent graft
Flinders Medical Center
Adelaide, Australia
RECRUITINGSingapore General Hospital
Singapore, Singapore
RECRUITINGPrimary Patency of Target Lesion (Cepahlic Arch)
Freedom from any re-intervention at target lesion that is clinically driven or indicated on surveillance scan
Time frame: 6-months post-op
Primary Patency of Access Circuit
Percentage of patients who do not need to undergo another re-intervention at the dialysis access circuit
Time frame: 6-months post-op
Primary Patency of Target Lesion
Percentage of patients who do not need to undergo another re-intervention at the target lesion
Time frame: 3 and 12 months post-op
Primary Patency of Access Circuit
Freedom from any re-intervention that is clinically driven or indicated on surveillance scan
Time frame: 3 and 12 months post-op
Assisted Primary Patency of Target Lesion
Percentage of patients who do not need to undergo another thrombolysis or thrombectomy at target lesion.
Time frame: 3 and 12 months post-op
Assisted Primary Patency of Access Circuit
Percentage of patients who do not need to undergo another thrombolysis or thrombectomy at dialysis access circuit
Time frame: 3 and 12 months post-op
Secondary Patency
Percentage of patients who will not need creation of a new AVF or an alternative dialysis access site.
Time frame: 3 and 12 months post-op
Time taken to next intervention
Time frame: 12-months post-op
Number of repeat interventions to target lesion
Time frame: 6 and 12 months post-op
Number of repeat interventions to maintain access circuit
Time frame: 6 and 12 months post-op
Rate of late lumen loss of the cephalic arch, proximal and distal stent edge
Time frame: 12 months post-op
Complication Rate
Time frame: 1, 3, 6 and 12 months post-op
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.