Actively Recruiting
Routine vs On-demand ECMO for Lung Transplantation
Led by Centre hospitalier de l'Université de Montréal (CHUM) · Updated on 2025-12-23
218
Participants Needed
4
Research Sites
218 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Lung transplantation is a complex procedure performed in patients with terminal lung disease. The transplant procedure stresses the patient's heart and lungs, which are already taxed by the underlying disease process. The heart-lung machine is occasionally used to support the patient and ensure adequate oxygen supply to other organs during the operation. It can be used routinely in all patients or selectively in patients who exhibit reduced oxygen supply to the remaining organs. This process, known as cardiopulmonary bypass (CPB), pumps blood out of the body to a heart-lung machine that removes carbon dioxide and returns oxygen-filled blood to the body. Although using the CPB increases the risk of bleeding, infection, and coagulation complications, it should still be considered in high-risk patients to compensate for more severe complications such as kidney failure and stroke caused by a lack of cardiopulmonary support. Extracorporeal membrane oxygenation (ECMO) is a recently developed CPB variation associated with fewer bleeding complications. It has recently replaced the traditional heart-lung machine as the preferred method of cardiopulmonary support during lung transplantation. Since ECMO is associated with fewer complications than standard CPB, many centers have increased their use of ECMO during lung transplantation. Some have even employed it routinely. However, there remains significant debate on how often it should be used. Therefore, the study's main objective is to compare the two approaches in lung transplantation, i.e., routine use versus selective use, and to determine if one approach is preferable to the other.
CONDITIONS
Official Title
Routine vs On-demand ECMO for Lung Transplantation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing lung transplant surgery
You will not qualify if you...
- Unable to provide consent for the study
- Previous lung retransplantation
- Multi-organ transplantation
- Contraindication to standard heparin anticoagulation (e.g., heparin-induced thrombocytopenia)
- Need for mandatory intraoperative cardiopulmonary support due to severe pulmonary hypertension with systolic pulmonary artery pressure ≥ 80 mm Hg or mean pulmonary artery pressure ≥ 55 mm Hg or pulmonary to systemic artery pressure ratio > 0.66
- Moderate to severe right ventricular dysfunction
- Left ventricular ejection fraction less than 45%
- Requirement for concomitant cardiac surgery such as coronary artery disease needing surgical grafting
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 4 locations
1
Univeristy of Alberta & Alberta Health Services
Edmonton, Alberta, Canada, T6G2G3
Not Yet Recruiting
2
Vancouver General Hospital
Vancouver, British Columbia, Canada
Not Yet Recruiting
3
University Health Network / Toronto General Hospiatl
Toronto, Ontario, Canada, M5G 1M1
Not Yet Recruiting
4
Centre Hospitalier de l'Universite de Montreal
Montreal, Quebec, Canada, H2X3E4
Actively Recruiting
Research Team
B
Basil Nasir, MD
CONTACT
A
Alex Moore, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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