跳至主要内容
临床试验/NCT06876415
NCT06876415招募中不适用

Monitoring of Occlusion Pressure and Esophageal Pressure to Guide Weaning From Venovenous ECMO in ARDS: a Randomized Controlled Study

Assistance Publique Hopitaux De Marseille5 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年7月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
5
主要终点
Duration of mechanical ventilation from ECMO decannulation to weaning from mechanical ventilation

研究概览

简要总结

In its most severe form, Acute Respiratory Distress Syndrome (ARDS) may require the use of veno-venous ECMO (vvECMO). While the criteria for vvECMO indication, ECMO settings, and ventilator management are relatively well-defined after the publication of the EOLIA trial and subsequent national or international guidelines, few studies have assessed the criteria and methods for weaning from vvECMO. Besides, advances in the understanding of the pathophysiology of mechanical ventilation (MV) weaning process have led to the development of specific monitoring tools for this phase.

Schematically, respiratory drive can be evaluated via the ventilator by measuring the pressure generated during a 100-millisecond expiratory occlusion (P0.1) and respiratory efforts through the measurement of esophageal pressure variation (delta Poeso).

Recent retrospective studies conducted on COVID-19 ARDS patients supported by vvECMO suggest a longer duration of mechanical ventilation for patients whose weaning and decannulation process was "forced," i.e., performed under conditions of significant respiratory drive and effort. High values of P0.1 and delta Poeso were associated with prolonged MV duration. Self-inflicted lung injury (P-SILI) and elevated transpulmonary pressure related to these uncontrolled respiratory efforts likely explain the negative impact on MV duration.

Therefore, this randomized study proposes to assess these monitoring tools, which are regularly used in clinical practice, to guide vvECMO weaning and decannulation decisions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Investigator)

盲法说明

P0.1 and delta Poeso values will be monitored in a blinded manner by an independent investigator and will not be integrated into the decannulation decision

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adult patients aged 18 years or older Patient whose trusted person has given consent for participation in the study
  • •Patient on veno-venous ECMO with weaning criteria, including:
  • •Resolution of the cause of ARDS
  • •Absence of hemodynamic instability, defined as norepinephrine dose ≤ 0.5 μg/kg/min for at least 3 hours
  • •Use of a ventilatory mode that allows spontaneous ventilation (VS-AI, BiPAP, or APRV)
  • •Maximum inspiratory pressure ≤ 28 cm H2O, with a maximum driving pressure ≤ 15 cm H2O, enabling tidal volumes between 4 and 8 ml/kg of predicted body weight (PBW)
  • •ECMO membrane sweep flow ≤ 2 L/min
  • •Patient protected by social security

排除标准

  • •Contraindication to the placement of an esophageal pressure balloon (e.g., esophageal varices, nasal trauma, uncontrolled coagulopathy, severe thrombocytopenia),
  • •Patient with treatment limitation at the time of inclusion,
  • •Patient in the time frame of exclusion from another research protocol at the time of consent signing,
  • •Vulnerable patients: minor, adult patient under guardianship or curatorship, patient deprived of liberty, pregnant or breastfeeding woman.

研究组 & 干预措施

ECMO-physio group

Experimental

Patients undergo the ultimate vvECMO weaning test with minimal ECMO support (ECMO flow ≤ 3 L/min, fresh gas flow ≤ 1 L/min, FiO2 21%) and mechanical ventilation with partial support, allowing spontaneous ventilation. P0.1 and delta Poeso values will be monitored and integrated into the decannulation decision

干预措施: P0.1 and delta Poeso integration into the decanulation decision (Other)

ECMO-gazo group

No Intervention

Patients undergo the ultimate vvECMO weaning test with minimal ECMO support, similar to the experimental group. P0.1 and delta Poeso values will be monitored in a blinded manner by an independent investigator and will not be integrated into the decannulation decision.

结局指标

主要结局

Duration of mechanical ventilation from ECMO decannulation to weaning from mechanical ventilation

时间窗: 60 days after inclusion

The weaning from mechanical ventilation is defined as the absence of mechanical ventilation for 48 consecutive hours.

P0.1 and delta Poeso measurements

时间窗: From inclusion to 48h after decanulation

P0.1 and delta Poeso values will be monitored and tracked at inclusion and then every 8 hours until decannulation, and up to 48 hours after decannulation. In the experimental group, these values will be incorporated into the criteria guiding the decannulation decision. In the control group, these values will be monitored and recorded by an investigator who is not involved in the decannulation decision. These values will not be included in the criteria guiding the decannulation decision.

次要结局

  • Number of patients who received corticosteroid therapy(60 days after inclusion)
  • Mortality rate in intensive care unit(60 days after inclusion)
  • Intensive care unit stay duration from inclusion(60 days after inclusion)
  • Total duration of mechanical ventilation(60 days after inclusion)
  • Time between the start of mechanical ventilation and ECMO cannulation(60 days after inclusion)
  • Number of ventilator-free days(60 days after inclusion)
  • Neuromyopathy on the day of decannulation(Day of decanulation)
  • Mortality rate in hospital(60 days after inclusion)
  • Hospital stay duration from inclusion(60 days after inclusion)
  • Total number of days spent on ECMO from admission to intensive care unit discharge(60 days after inclusion)
  • Number of patients decannulated and then re-initiated on vvECMO(60 days after inclusion)
  • Number of patients requiring controlled ventilation for at least 24 hours after decannulation(60 days after inclusion)
  • Number of days with continuous sedation with or without continuous paralysis after decannulation(60 days after inclusion)
  • Incidence of barotrauma assessed by radiographs and clinical examination after decannulation(60 days after inclusion)
  • Percentage of patients placed in prone positioning after decannulation(60 days after inclusion)
  • Number of days on inhaled nitric oxide after decannulation(60 days after inclusion)
  • Neuromyopathy on the day of weaning from mechanical ventilation(Day of weaning from mechanical ventilation)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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