RECOMMEND Platform Trial
Launched by AUSTRALIAN AND NEW ZEALAND INTENSIVE CARE RESEARCH CENTRE · Jul 25, 2024
Trial Information
Current as of July 22, 2025
Not yet recruiting
Keywords
ClinConnect Summary
The RECOMMEND Platform Trial is a research study designed to improve care for patients on extracorporeal membrane oxygenation (ECMO), a treatment used in the intensive care unit (ICU) to help patients with severe breathing problems. The goal of the trial is to create better guidelines and evidence for ECMO care, so doctors can make more informed decisions based on the latest research. This trial will also allow researchers to test different treatment options at the same time, making it easier and faster to find out what works best for patients.
To participate in this trial, patients must be receiving ECMO and enrolled in a specific registry called the EXCEL Registry. Unfortunately, if a doctor believes that death is imminent for a patient or that participating in the trial may not be in the patient’s best interest, they will not be eligible. While the trial is not yet recruiting participants, it emphasizes the importance of patient preferences and aims to provide valuable insights to improve outcomes for those receiving ECMO care.
Gender
ALL
Eligibility criteria
- PLATFORM INCLUSION CRITERIA:
- • Patients receiving ECMO
- • Patients enrolled in the EXCEL Registry - NCT03793257
- PLATFORM EXCLUSION CRITERIA:
- • Treating clinician regards death as imminent and inevitable
- • Treating clinician determines it is not in the patient's best interests
- RBC TRANSFUSION DOMAIN INCLUSION CRITERIA:
- • • Aged 18 years or older
- RBC TRANSFUSION DOMAIN EXCLUSION CRITERIA:
- • Contraindication to RBC transfusion (including known patient preference)
- • Limitations of care put in place either through patient wishes or the treating medical teams.
- • Participant has already received ECMO \>12 hours. The start of ECMO is defined as the time of initiation of extracorporeal blood flow unless ECMO was initiated during a surgical intervention in which case the start of ECMO is defined as the arrival time into the initial ICU (post-surgery)
- • The treating physician anticipates that ECMO treatment will cease before the end of tomorrow
- • The treating physician deems the study is not in the patient's best interest
- • The treating physician has concern regarding patient ability to tolerate restrictive or liberal transfusion trigger thresholds
- • Actively listed for a solid organ transplant and has not yet received one
- • Suspected or confirmed to be pregnant
- • Previous ECMO treatment during the same hospital admission
About Australian And New Zealand Intensive Care Research Centre
The Australian and New Zealand Intensive Care Research Centre (ANZIC-RC) is a leading research organization dedicated to improving outcomes in critically ill patients through innovative clinical trials and research initiatives. Based at Monash University, the Centre fosters collaborative partnerships among clinicians, researchers, and institutions across Australia and New Zealand. Its focus on evidence-based practice and translational research aims to enhance the quality of intensive care, drive advancements in treatment protocols, and ultimately improve patient care in the intensive care unit (ICU) setting. ANZIC-RC is committed to addressing key challenges in critical care medicine, ensuring that findings from its trials contribute to better health outcomes and inform clinical guidelines globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Melbourne, Victoria, Australia
Camperdown, New South Wales, Australia
Sydney, New South Wales, Australia
Patients applied
Trial Officials
Carol Hodgson, PhD FACP FAHMS
Study Chair
Monash University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported