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

Author:

D'Aragon FrederickORCID,Selzner Markus,Breau Ruth,Masse Marie-Hélène,Lamontagne Francois,Masse Mélanie,Chassé Michael,Carrier François-Martin,Cardinal Héloïse,Chaudhury Prosanto,Weiss MatthewORCID,Lauzier FrancoisORCID,Turgeon Alexis FORCID,Frenette Anne-Julie,Bolduc Brigitte,Ducharme Anique,Lamarche Caroline,Couture EtienneORCID,Holdsworth Sandra,Bertholz Liz,Talbot Heather,Slessarev Marat,Luke Patrick,Boyd John Gordon,Shamseddin M Khaled,Burns Karen E A,Zaltzman Jeffrey,English Shane,Knoll Greg,Dhanani Sonny,Healey Andrew,Hanna Steven,Rochwerg Bram,Oczkowski Simon J W,Treleaven Darin,Meade Maureen

Abstract

IntroductionMost 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 analysisWe 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 disseminationWe 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 numberNCT05148715.

Publisher

BMJ

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