跳至主要内容
临床试验/NCT07189078
NCT07189078招募中不适用

IntHyx : Intubation Strategies for Patients With Acute Hypoxemic Respiratory Failure

University Hospital, Angers9 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2025年12月13日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
200
试验地点
9
主要终点
Impact of a liberal intubation strategy compared to a restrictive strategy in regards to organ support duration, taking mortality into account

研究概览

简要总结

Acute hypoxemic respiratory failure requires endotracheal intubation and invasive mechanical ventilation in approximately 30-40% of cases, due to severe hypoxemia and/or clinical signs of acute respiratory distress. The primary objectives of invasive mechanical ventilation are to reduce respiratory effort and improve oxygenation. However, this intervention is also associated with both direct and indirect adverse effects, mainly linked to the need for sedation and often neuromuscular blockade. These include hemodynamic compromise, neuromuscular weakness, ventilator-induced lung injury, and infectious complications.

An ideal intubation strategy would therefore strike a balance: avoiding the risks of delayed intubation-such as refractory hypoxemia, excessive respiratory effort, and patient self-inflicted lung injury (P-SILI)-while limiting complications associated with invasive mechanical ventilation by withholding it in patients who might otherwise recover without. To date, the optimal strategy for achieving this risk-benefit balance remains uncertain.

Clinical practice suggests a broad consensus on the necessity of intubation when so-called safety criteria are met: severe hypoxemia (SaO₂/FiO₂ ratio < 88), marked respiratory distress (use of accessory muscles, thoracoabdominal paradox, respiratory rate > 40/min), extra-respiratory manifestations of hypoxia (e.g., altered consciousness), and/or uncontrolled hemodynamic instability. Beyond these safety thresholds, however, debate persists. Some advocate for earlier intubation-a so-called liberal approach-triggered by predefined hypoxemia criteria (e.g., SpO₂/FiO₂ < 110), with the aim of limiting the deleterious consequences of sustained hypoxemia.

In routine practice, the criteria guiding intubation vary widely between clinicians and cannot be attributed to strong scientific evidence. This study therefore seeks to compare, in a randomized interventional design, the two main strategies currently applied across centers:

  • Liberal intubation strategy: prioritizing the prevention of organ dysfunction related to hypoxemia (notably hypoxic cardiac arrest) and the risk of P-SILI.
  • Restrictive intubation strategy: prioritizing the reduction of invasive mechanical ventilation use, with the goal of minimizing ventilation-related harm and its associated therapeutic burden.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Adult patient
  • Patient admitted to intensive care less than 24 hours ago
  • Acute respiratory failure with hypoxemia defined by either:
  • Oxygen therapy ≥ 10 L/min via high-concentration mask required for 92 ≤ SpO2 ≤ 98%
  • High-flow oxygen therapy with FiO2 ≥ 50% required for 92 ≤ SpO2 ≤ 98%
  • Informed consent of the patient or a trusted relative (when the patient is unable to give consent)

排除标准

  • Acute hypercapnic respiratory failure (defined by PaCO2 > 45 mmHg)
  • Cardiogenic pulmonary edema
  • Exacerbation of chronic respiratory disease
  • Respiratory failure requiring long-term oxygen therapy
  • Neuromuscular disease
  • Glasgow Coma Scale score ≤ 12
  • Decision to intubate immediately
  • Invasive mechanical ventilation within the previous 7 days
  • Treatment limitation decisions for intubation
  • Person deprived of liberty by judicial or administrative decision : Person undergoing compulsory psychiatric care, person subject to legal protection measures, Pregnant, breastfeeding, or parturient patient

研究组 & 干预措施

"Liberal" intubation strategy

Experimental

Endotracheal intubation is recommended if SpO₂/FiO₂ < 110 for more than 5 minutes.

In addition, intubation is also recommended in the liberal strategy if any of the restrictive strategy criteria occur and persist for more than 5 minutes.

干预措施: Liberal intubation strategy (Procedure)

Restrictive intubation strategy

Experimental

Endotracheal intubation is recommended only if at least one of the following criteria persists for more than 5 minutes:

  1. Respiratory rate > 40/min, persistent use of accessory muscles, or thoracoabdominal paradox.
  2. SpO₂/FiO₂ < 88.
  3. Neurological or systemic impairment attributable to hypoxemia, defined as: altered higher brain functions without another identifiable cause, Glasgow Coma Scale ≤ 12, uncontrolled hemodynamic instability, or rising lactate levels.

干预措施: Restrictive intubation strategy (Procedure)

结局指标

主要结局

Impact of a liberal intubation strategy compared to a restrictive strategy in regards to organ support duration, taking mortality into account

时间窗: Day 28

Composite endpoint consisting of death and number of days with organ failure at D28, analyzed using the Win Ratio method.

次要结局

  • Estimated tidal volume by Electrical impedance tomography (EIT)(1 hour, 24 hours, and 48 hours after enrollment)
  • Evaluate the impact of the intubation strategy on intubation rates over time.(Day 28)
  • Assess the impact of the intubation strategy on each component of the composite primary endpoint.(Day 28)
  • Assess the impact of the intubation strategy on the severity of vital organ failure and the duration of care.(Day 28)
  • Assess the impact of the intubation strategy on the rate of procedure-related adverse events.(within 30 minutes of the start of the intubation procedure)
  • Assess the impact of the intubation strategy on the rate of adverse events related to invasive mechanical ventilation.(Day 28)
  • Assess the impact of the intubation strategy on quality of life at day 90.(Day 90)
  • Assess the impact of the intubation strategy on the rate of adverse events potentially related to delayed intubation.(Day 28)

研究者

发起方
University Hospital, Angers
申办方类型
Other Gov
责任方
Sponsor

研究点 (9)

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