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Clinical Trial Summary

The study investigators propose to perform a blood test before and after allograft placement in all patients receiving a cold-stored venous allografts at the University Hospital of Nîmes to study the occurrence of FVFA-related ASD in these patients. The aim of this work is to characterize a possible immune reaction generated by the implantation of venous allografts prepared according to the BIOPROTEC method. In case of a proven immune reaction, the study will allow a modification of our current attitude and to exclude patients potentially eligible for renal transplantation at the time of venous allograft placement, or to perform in these patients an allo-compatibility test with the venous allograft preoperatively and thus protect these patients from an increased risk of subsequent organ transplant rejection.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05096351
Study type Observational
Source Centre Hospitalier Universitaire de Nimes
Contact Elsa Faure
Phone 04.66.68.39.30
Email elsa.faure@chu-nimes.fr
Status Recruiting
Phase
Start date June 8, 2022
Completion date December 2025

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