Clinical Trial

Controlled Terminal Reperfusion With Cold Preservation Solution in the cDCD III Donor

Study acronym: PERFEND
Completed
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Summary
The goal of this observational study is to describe the details of a controlled administration strategy of cold preservation solution or oxygenated cold preservation solution at the end of Abdominal Normothermic Regional Perfusion (A-NRP) in Controlled Donation afeter Circulatory determination of Death (cDCD) III donors. The main purpose is to: develope a standardized protocol for this type of donor Data collected from partecipants, deceased donors belonging to cDCD III category, willl be analysed through descriptive stastistics.
Trial Details
NCT Number NCT07421726
Lead Sponsor IRCCS Azienda Ospedaliero-Universitaria di Bologna
Conditions Transplant Patients, Organ Failure, Multiple, Organ Donor Registration
Enrollment 20 participants
Start Date 2025-03-17
Primary Completion 2025-12-16 (estimated)
Study Completion 2025-12-16 (estimated)
Updated on ClinicalTrials.gov 2026-02-19