Dialysis patients presenting for angioplasty intervention for graft failure will be randomized to receive either Sirolimus or not receive Sirolimus (standard of care) to assess the time from primary failure or angioplasty intervention to second or next angioplasty intervention or graft failure.
This is a randomized control study to determine the feasibility of using sirolimus peri-angioplasty to compare the time from primary failure or angioplasty intervention to second or next angioplasty intervention or graft failure to a control group who would not have received Sirolimus
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
17
3 mg po od loading dose for two days, then 2 mg po od for thirty days
London Health Sciences Centre
London, Ontario, Canada
Comparison of the sirolimus group to the control group from time of assisted primary and secondary patency rates to access abandonment
Comparison of the sirolimus group to the control group from time of assisted primary and secondary patency rates to access abandonment
Time frame: 12 months
Secondary End point
Secondary end points will be improvement in vascular access flow rates as measured by either online conductivity dialysance or ultrasound dilution techniques.
Time frame: 12 months
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