Clinical Trials Directory

Trials / Completed

CompletedNCT04569682

Outcomes of Transrenal Artery Perfusion Versus Transrenal Vein Perfusion Using LifePort for Deceased Donor Kidney Transplantation

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
108 (actual)
Sponsor
West China Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The main objective of this study is to compare the outcomes of transrenal artery perfusion versus transrenal vein perfusion using LifePort for deceased donor kidney transplantation. Patients registered in the National Dialysis and Transplant Registry awaiting deceased donor kidney transplantation were included. Delayed graft function (DGF) or primary nonfunction (PNF) may occur after deceased donor kidney transplantation. Compared with static cold storage, the application of LifePort can significantly reduce the incidence of DGF and PNF in deceased donor kidney transplantation. Transrenal artery perfusion is currently the mainstream but confronts multiple renal arteries, resulted in prolonged cold ischemia time. Transrenal vein perfusion is expected to be a solution. However, whether the clinical outcomes of transrenal vein perfusion is inferior to transrenal artery perfusion remains unknown. In this study, values of urine volume and creatinine, incidence and duration of DGF, and incidence of PNF within 1 week after surgery are recorded and compared between the transrenal artery perfusion group and the transrenal vein perfusion group. Monthly eGFR and creatinine values, the incidence of acute rejection within 1 year after transplantation and 1-year graft and patient survival are also recorded and compared.

Conditions

Interventions

TypeNameDescription
DEVICELifePort transrenal artery perfusiontransrenal artery perfusion group
DEVICELifePort transrenal vein perfusiontransrenal vein perfusion group

Timeline

Start date
2020-01-01
Primary completion
2021-10-30
Completion
2022-12-30
First posted
2020-09-30
Last updated
2023-05-22

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04569682. Inclusion in this directory is not an endorsement.