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Study identifier: NCT05425056 Synced from ClinicalTrials.gov · July 28, 2026
● Completed

A Study Testing the Use of a Perivascular Sirolimus Formulation (Sirogen) in ESRD Patients Undergoing AV Fistula Surgery

Condition: Complication of Renal Dialysis · End Stage Renal Disease · End Stage Kidney Disease  ·  Sponsor: Vascular Therapies, Inc.

PhasePhase 3
Planned participants136
Who can joinAll sexes, 65 Years to no upper limit
Healthy volunteersNo

About this study

The primary study objective is to evaluate the benefit of the Sirolimus eluting Collagen implant (SeCI; Sirogen), a single dose prophylactic treatment delivered intraoperatively at the time of surgical creation of an arteriovenous fistula for hemodialysis vascular access.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (22)

Veterans Affairs San Diego Health CenterSan Diego, California, United States
Lundquist Institute for Biomedical InnovationTorrance, California, United States
MedStar Cardiovascular Research Network at MedStar Washington Hospital CenterWashington D.C., District of Columbia, United States
American Access Care of MiamiMiami, Florida, United States
Emory University Hospital MidtownAtlanta, Georgia, United States
Augusta UniversityAugusta, Georgia, United States
University of LouisvilleLouisville, Kentucky, United States
The Brigham and Women's HospitalBoston, Massachusetts, United States
Mount Sinai HospitalNew York, New York, United States
Atrium HealthCharlotte, North Carolina, United States
Surgical Specialists of CharlotteCharlotte, North Carolina, United States
The Regional Medical Center/Dialysis Access InstituteOrangeburg, South Carolina, United States

+ 10 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05425056