RECOMMEND Platform Trial

EARLY_PHASE1NOT_YET_RECRUITING

Patients in the intensive care unit (ICU) undergoing extracorporeal membrane oxygenation (ECMO) require close monitoring and interventions to support their recovery. The RECOMMEND Platform Trial aims to develop clear, high-quality evidence for ECMO care, to better inform clinicians in this rapidly evolving field. The RECOMMEND Platform Trial will provide a 'platform' for funding, logistics, and training protocols.

This approach enhances efficiency, allowing research to begin, and complete more efficiently. The platform maintains rigorous standards and provides a safe, cost-effective, and time-efficient method for generating knowledge about ECMO care. Overall, platform clinical trials offer a dynamic and innovative approach that enables the simultaneous evaluation of multiple treatments and the rapid translation of scientific discoveries into improved patient care.

The RECOMMEND Platform Trial has been informed by patient preferences and values and will evaluate the effectiveness and safety of various standards of care. This approach supports continuous learning and real-time clinical decision-making to improve patient outcomes.

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Study details:

The RECOMMEND Platform trial is an investigator initiated, multicentre, open labelled, randomised controlled Platform Trial that will utilise Bayesian adaptive logic to investigate the efficacy and safety of multiple study interventions simultaneously or sequentially in cohorts of adult patients who are receiving ECMO from ICUs participating in the national ECMO registry (EXCEL) in Australian and New Zealand ICU hospitals. In this platform trial, various interventions within the scope of standard care will be investigated for their potential to improve outcomes for patients undergoing ECMO. Standard care will be used as the common control arm for all intervention cohorts.

Extracorporeal Membrane Oxygenation (ECMO) is an invasive and resource intensive treatment used to support critically ill patients suffering from severe cardiac arrest, cardiac failure or respiratory failure. ECMO provides mechanical circulatory support, temporarily replacing the function of the heart and/or lungs, allowing time for these organs to recover. Globally, the use of ECMO has increased rapidly over the past decade.

It is both invasive and expensive, with the average cost for a single admission in Australia exceeding more than $180,000 and a total annual cost of \> $75 million. Despite its high cost, ECMO is associated with a high mortality rate, and many survivors have compromised functional recovery for months or years after discharge from hospital, further adding to the long-terms costs of care. The main complications reported in the national ECMO registry from 2019-2022 include bleeding (51.

4%), renal failure and fluid overload (78. 4%), and death and ongoing disability (66%). These were confirmed as research priorities by consumers and end-users.

While the use of ECMO increases swiftly, the evidence base to support the growing patient numbers receiving this care has not grown at the same rate, resulting in important evidence gaps. The RECOMMEND Platform Trial will address these evidence gaps in ECMO services in Australia. A platform trial is a type of study design that evaluates multiple treatment interventions for a single condition or device simultaneously within a single, overarching framework.

This framework operates similarly to a standard operating procedure for study logistics, ethics management, funding, staffing, and statistical and data collection methods. Having an approved process (platform) for the 'Platform Trial' to operate saves time and money and increases speed of clinical trial onboarding to outcome resolution for researchers, hospital staff, ethics committees, and stakeholders. With this platform in place, future studies of similar ECMO outcomes can be onboarded more efficiently, as described above, and it creates a more powerful pool of data for impactful patient-centred research.

The aim of the RECOMMEND Platform Trial is to determine, in patients with acute cardiorespiratory failure requiring ECMO, the efficacy, safety and cost-effectiveness of a range of interventions. Over the lifetime of RECOMMEND, it is anticipated that new interventions will be added as new domains. The creation of new domains will be considered according to priorities set by relevant working groups, based on existing or new clinical need and there being sufficient statistical power available within RECOMMEND.

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Eligibility criteria

Researchers look for people who fit a certain description, called eligibility criteria. See if you qualify.

Inclusion criteria

  • Patients receiving ECMO
  • Patients enrolled in the EXCEL Registry
  • Exclusion criteria

  • Treating clinician regards death as imminent and inevitable
  • Treating clinician determines it is not in the patient's best interests
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    Eligibility

    Age eligible for study : 0 and older

    Healthy volunteers accepted : Yes

    Gender eligible for study: All

    Things to know

    Study dates

    Study start: 2024-09-01

    Primary completion: 2028-05-31

    Study completion finish: 2028-11-30

    study type

    Study type

    SUPPORTIVE_CARE

    phase

    Phase

      EARLY_PHASE1

    trial

    Trial ID

    NCT06526533

    Intervention or treatment

    OTHER: Liberal Transfusion

    OTHER: Restrictive Transfusion

    Conditions

    • Extracorporeal Membrane Oxygenation Complication
    Image related to Extracorporeal Membrane Oxygenation Complication
    • Condition: Extracorporeal Membrane Oxygenation Complication

    • OTHER: Liberal Transfusion and other drugs

    • Camperdown, New South Wales, Australia and more

    • Sponsor: Australian and New Zealand Intensive Care Research Centre

    Find a site

    Closest Location:

    Royal Prince Alfred Hospital

    Research sites nearby

    Select from list below to view details:

    • Royal Prince Alfred Hospital

      Camperdown, New South Wales, Australia

    • The Alfred Hospital

      Melbourne, Victoria, Australia

    • St. Vincent's Hospital Sydney

      Sydney, New South Wales, Australia

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    Study Plan

    This section provides details of the study plan, including how the study is designed and what the study is measuring.

    How is the study designed?

    Participant Group/ArmIntervention/Treatment
    ACTIVE_COMPARATOR: Blood Transfusion Domain: Red Blood Cell Transfusion in ECMO - Restrictive
    • This is a domain within the RECOMMEND Platform Trial to test the effectiveness of various blood transfusion strategies for patients with acute cardiorespiratory failure undergoing ECMO treatment in ICU.
    • Arm details:
    • The Australian Blood Authority's guidelines recommend a transfusion trigger of haemoglobin (Hb) levels between 70g/L and 90g/L for critically ill patients in ICU. However, this range is broad, and allows great variation in standard care. ROSETTA is a comparative effectiveness trial, assigning patients to two intervention groups that are in the realm of standard care. Participants are patients receiving extracorporeal membrane oxygenation (ECMO) in ICU who are eligible for inclusion in the EXCEL National ECMO Registry.
    • Trigger:
    • If a patient's Hb concentration reads ≤ 70g/L, one unit of RBC will be transfused. Additional units can be prescribed if required to raise the Hb concentration to above 70g/L.
    OTHER: Restrictive Transfusion
    • Restrictive transfusion trigger group (patient receives RBC transfusion if Hb≤70g/L).
    ACTIVE_COMPARATOR: Blood Transfusion Domain: Red Blood Cell Transfusion in ECMO - Liberal
    • This is a domain within the RECOMMEND Platform Trial to test the effectiveness of various blood transfusion strategies for patients with acute cardiorespiratory failure undergoing ECMO treatment in ICU.
    • Arm details:
    • The Australian Blood Authority's guidelines recommend a transfusion trigger of haemoglobin (Hb) levels between 70g/L and 90g/L for critically ill patients in ICU. However, this range is broad, and allows great variation in standard care. ROSETTA is a comparative effectiveness trial, assigning patients to two intervention groups that are in the realm of standard care. Participants are patients receiving extracorporeal membrane oxygenation (ECMO) in ICU who are eligible for inclusion in the EXCEL National ECMO Registry.
    • Trigger:
    • If a patient's Hb concentration reads ≤ 90g/L, one or more units of RBC will be transfused. Additional units can be prescribed to raise the Hb concentration to greater than 90g/L
    OTHER: Liberal Transfusion
    • Liberal transfusion trigger group (patient receives RBC transfusion if Hb ≤ 90g/L).

    What is the study measuring?

    Primary outcome

    Primary Outcome MeasurePrimary Outcome DescriptionPrimary Outcome Time Frame
    Daily Organ Support for patients on ECMO (DOSE-score).The primary outcome is the Daily Organ Support for patients on ECMO (DOSE-score), a 6-level daily ordinal outcome measured as the worst status of a patient on each day from day 1 through to day 28 inclusive, which reflects survival, organ support and resource utilisation: 1. dead; 2. on ECMO; 3. invasively mechanically ventilated without ECMO; 4. in ICU but not invasively mechanically ventilated nor on ECMO; 5. in hospital; and 6. discharged from the hospital alive.28-days.

    Secondary outcome

    Secondary Outcome MeasureSecondary Outcome DescriptionSecondary Outcome Time Frame
    ECMO-related bleeding and thrombotic complications at 28-days.Development of major ECMO-related bleeding and thrombotic complications (e.g. stroke, major haemorrhage, amputation).28-days.
    Mortality at 28-days.Living status.28-days.
    ECMO-free days at 28-days.Number of days not receiving ECMO.28-days.
    Ventilator-free days at 28-days.Number of days not receiving ventilation.28-days.

    Frequently Asked Questions

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    References

    Clinical Trials Gov: RECOMMEND Platform Trial

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