Project 461194
The effects of an intraoperative targeted low-splanchnic blood volume restrictive fluid management strategy compared to a liberal one on postoperative outcomes in liver transplantation - the REFIL (REstrictive Fluid management In Liver transplantation) pilot multicenter randomized controlled trial
The effects of an intraoperative targeted low-splanchnic blood volume restrictive fluid management strategy compared to a liberal one on postoperative outcomes in liver transplantation - the REFIL (REstrictive Fluid management In Liver transplantation) pilot multicenter randomized controlled trial
Project Information
| Study Type: | Unclear |
| Research Theme: | Clinical |
Institution & Funding
| Principal Investigator(s): | Carrier, François M; Chasse, Michael; Fergusson, Dean A |
| Co-Investigator(s): | Chaudhury, Prosanto K; Giard, Jeanne-Marie; Gonzalez Valencia, Nelson J; Kandelman, Stanislas; Karvellas, Constantine J; Martel, Guillaume; Schnitzer, Mireille E; Simoneau, Eve B; Thavorn, Kednapa |
| Institution: | Centre hospitalier de l'Université de Montréal (CHUM) |
| CIHR Institute: | Health Services and Policy Research |
| Program: | |
| Peer Review Committee: | Clinical Investigation - C: Digestive, Endocrine and Excretory Systems |
| Competition Year: | 2022 |
| Term: | 2 yrs 6 mths |
Abstract Summary
Liver transplantation is a life-saving procedure for patients with end-stage liver disease, but it carries a high risk of complications. About 60% of liver transplant recipients suffer from a severe postoperative complication. Few perioperative interventions (conducted just before, during or just after the surgery) have been shown to reduce these complications in liver transplantation. Blood volume management and intravenous fluid administration is an important aspect of anesthesia and perioperative care in this population. A restrictive approach to fluid administration has been suggested to improve outcomes. We propose to compare the effects of an intraoperative restrictive fluid management strategy to a more liberal one on major postoperative complications, mortality and quality of life in adult liver transplantation. Since no Canadian multicenter perioperative clinical trial has ever been undertaken in this population, we propose to conduct a pilot multicenter randomized controlled feasibility trial. If feasibility of such a trial is confirmed, a future efficacy trial will be completed to answer this important research question.
No special research characteristics identified
This project does not include any of the advanced research characteristics tracked in our database.