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Calcineurin Inhibitor in NEuRoloGically deceased donors to decrease kidney delayed graft function study: study protocol of the CINERGY Pilot randomised controlled trial

Authors :
Greg Knoll
Bram Rochwerg
François Lauzier
Marat Slessarev
Michaël Chasse
Karen E A Burns
Alexis F Turgeon
John Gordon Boyd
Frédérick D'Aragon
Shane English
Matthew Weiss
Maureen Meade
Sonny Dhanani
Marie-Hélène Masse
François-Martin Carrier
Steven Hanna
Andrew Healey
Simon J W Oczkowski
Anne-Julie Frenette
Anique Ducharme
Prosanto Chaudhury
Markus Selzner
Ruth Breau
Mélanie Masse
Héloïse Cardinal
Brigitte Bolduc
Caroline Lamarche
Etienne Couture
Sandra Holdsworth
Liz Bertholz
Heather Talbot
Patrick Luke
M Khaled Shamseddin
Jeffrey Zaltzman
Darin Treleaven
Source :
BMJ Open, Vol 14, Iss 6 (2024)
Publication Year :
2024
Publisher :
BMJ Publishing Group, 2024.

Abstract

Introduction Most solid organ transplants originate from donors meeting criteria for death by neurological criteria (DNC). Within the organ donor, physiological responses to brain death increase the risk of ischaemia reperfusion injury and delayed graft function. Donor preconditioning with calcineurin inhibition may reduce this risk.Methods and analysis We designed a multicentre placebo-controlled pilot randomised trial involving nine organ donation hospitals and all 28 transplant programmes in the Canadian provinces of Ontario and Québec. We planned to enrol 90 DNC donors and their approximately 324 organ recipients, totalling 414 participants. Donors receive an intravenous infusion of either tacrolimus 0.02 mg/kg over 4 hours prior to organ retrieval, or a matching placebo, while monitored in an intensive care unit for any haemodynamic changes during the infusion. Among all study organ recipients, we record measures of graft function for the first 7 days in hospital and we will record graft survival after 1 year. We examine the feasibility of this trial with respect to the proportion of all eligible donors enrolled and the proportion of all eligible transplant recipients consenting to receive a CINERGY organ transplant and to allow the use of their health data for study purposes. We will report these feasibility outcomes as proportions with 95% CIs. We also record any barriers encountered in the launch and in the implementation of this trial with detailed source documentation.Ethics and dissemination We will disseminate trial results through publications and presentations at participating sites and conferences. This study has been approved by Health Canada (HC6-24-c241083) and by the Research Ethics Boards of all participating sites and in Québec (MP-31-2020-3348) and Clinical Trials Ontario (Project #3309).Trial registration number NCT05148715.

Subjects

Subjects :
Medicine

Details

Language :
English
ISSN :
20446055
Volume :
14
Issue :
6
Database :
Directory of Open Access Journals
Journal :
BMJ Open
Publication Type :
Academic Journal
Accession number :
edsdoj.0da023b6c5d4443aad540ffec3e61c6c
Document Type :
article
Full Text :
https://doi.org/10.1136/bmjopen-2024-086777