Dennis, Brittany
Deane, Adam
Lauzier, François
Zytaruk, Nicole
Hardie, Miranda
Hammond, Naomi
Finfer, Simon
Arabi, Yaseen
Marshall, John
Saunders, Lois
Heels-Ansdell, Diane
Myburgh, John
Knowles, Serena
Muscedere, John
Ostermann, Marlies
Rajbhandari, Dorrilyn
English, Shane
Matic, Karlo
Venkatesh, Bala
Al Fares, Abdulrahman
Guyatt, Gordon
Alhazzani, Waleed
Mumtaz, Hassan
Poole, Alexis
Xie, Feng
Thabane, Lehana
Hall, Richard
Cook, Deborah
Funding for this research was provided by:
Canadian Institutes of Health Research (202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215, 202207CL3-492565-CTP-CEBA-19215)
Physicians' Services Incorporated Foundation (R2-33, R2-33, R2-33, R2-33)
Hamilton Academy of Health Sciences Organization (HAH-22-009, HAH-22-009, HAH-22-009, HAH-22-009, HAH-22-009, HAH-22-009, HAH-22-009, HAH-22-009, HAH-22-009, HAH-22-009, HAH-22-009)
Article History
Received: 13 June 2023
Accepted: 23 April 2024
First Online: 4 May 2024
Declarations
:
: The Hamilton Integrated Research Ethics Board (HiREB) approved the REVISE trial. REVISE was also approved by relevant research ethics committees as required in each jurisdiction. All experiments were performed in accordance with relevant guidelines and regulations. Informed consent models approved for REVISE pre-pandemic included a priori consent and consent to continue. Where possible, informed a priori consent was obtained for all participants or their substitute decision maker. Consent to continue models were also employed. In cases where participants were unable to provide consent and lacked a substitute decision maker, consent to continue models were employed. Not all participants are able to provide informed consent given the nature of the included population.
: Not applicable for this publication. REVISE is a trial endorsed by the ANZICS-Clinical Trials Group and the Canadian Critical Care Trials Group.
: The authors declare no competing interests.