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Results of Cold Stored Allografts in Vascular Access (RAVASC)

C

Central Hospital, Nancy, France

Status

Completed

Conditions

End Stage Renal Failure on Dialysis
Hemodialysis Access Failure

Treatments

Procedure: Vascular access by pass using a cold stored venous allograft

Study type

Observational

Funder types

Other

Identifiers

NCT04446546
2020PI096

Details and patient eligibility

About

Vascular access creation in patients with renal failure requiring long-term hemodialysis can be a challenge when there is no more autologous material or in case of infection, in a population undergoing long term dialysis with a longer life-expectancy. Many types of grafts have been used, with its advantages and drawbacks, such as prosthetic grafts (PTFE). Over the past decade, surgeons have used cold stored venous allografts as a biological conduit for hemodialysis, with the idea of avoiding most of major complications including a lower incidence of infection and steal syndrome, with patencies at least equivalent to PTFE. There is only a few data in the litterature, but many surgical teams use it when there is no autologous material or in case of infection.

The aim of the study is to give the primary patency of vascular access with this technique, and to assess its long term outcomes.

Enrollment

120 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • End stage renal failure patient requiring hemodialysis
  • With the placement of a venous allograft for a hemodialysis approach
  • Who underwent a surgery between January 1, 2014 and December 31, 2018 in a vascular surgery department participating in our study

Exclusion criteria

  • Patient <18 years old, or under guardianship / curatorship
  • Patient objecting to the use of his personal data in the context of research

Trial design

120 participants in 1 patient group

Cold Stored Allograft Vascular Access
Treatment:
Procedure: Vascular access by pass using a cold stored venous allograft

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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