跳至主要内容
临床试验/NCT06526533
NCT06526533招募中3 期

Generating New Evidence to Reduce Major Complications to Improve the Safety and Efficacy of ECMO in Severe Cardiac and Respiratory Failure (RECOMMEND)

Australian and New Zealand Intensive Care Research Centre6 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2026年3月23日最近更新:
干预措施

试验速览

阶段
3 期
状态
招募中
入组人数
600
试验地点
6
主要终点
Daily Organ Support for patients on ECMO (DOSE-score).

研究概览

简要总结

The goal of this platform trial is to determine the efficacy, safety and cost-effectiveness of various interventions in patients with acute cardiorespiratory failure requiring extracorporeal membrane oxygenation (ECMO)

The main question the platform trial aims to address is to determine the effect of a range of interventions on survival, organ support and resource utilisation to day 28 for hospitalised patients receiving ECMO.

Researchers will compare various interventions within multiple platform trial domains to see if the interventions have effects on survival, organ support and resource utilisation for the patient cohort.

Participants will be enrolled in accordance with the platform trial's domain structure to answer the research questions.

详细描述

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 hospitals (EXCEL Registry NCT03793257).

In this platform trial, various interventions will be investigated for their potential to improve outcomes for patients undergoing ECMO.

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Supportive Care
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • PLATFORM INCLUSION CRITERIA:
  • Patients receiving ECMO
  • Patients enrolled in the EXCEL Registry - NCT03793257

排除标准

  • 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

研究组 & 干预措施

Participant Group/Arm

Other

RBC Transfusion Domain:

Patients on ECMO in ICU enrolled in the RBC Transfusion Domain of RECOMMEND. Patients receive one of two RBC transfusion strategies (restrictive or liberal)

干预措施: Liberal RBC Transfusion (Other)

Participant Group/Arm

Other

RBC Transfusion Domain:

Patients on ECMO in ICU enrolled in the RBC Transfusion Domain of RECOMMEND. Patients receive one of two RBC transfusion strategies (restrictive or liberal)

干预措施: Restrictive RBC Transfusion (Other)

结局指标

主要结局

Daily Organ Support for patients on ECMO (DOSE-score).

时间窗: 28-days.

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.

次要结局

  • Development of major haemorrhage at 28 days(28-days.)
  • Development of intracranial haemorrhage at 28 days(28 days)
  • Mortality at 28 days(28 days)
  • ECMO-free days at 28 days(28 days)
  • Ventilator-free days at 28 days(28 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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