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Predicting High-Flow Nasal Cannula Failure in Acute Hypoxemic Respiratory Failure Using Metabolomics and Clinical Data (META-RESPIRE)

2026年6月4日 更新者:Andrea Castellvi、Hospital del Mar Research Institute (IMIM)

Metabolomics and Clinical Data to Predict High-Flow Nasal Cannula Failure and Optimize Respiratory Support in Acute Hypoxemic Respiratory Failure

The goal of this observational study is to determine whether metabolomic profiles combined with clinical data can predict high-flow nasal cannula (HFNC) failure and help optimize respiratory support in adult patients with acute hypoxemic respiratory failure (AHRF). The main questions it aims to answer are:

Can metabolomic biomarkers identify patients at higher risk of HFNC failure? Does combining metabolomic and clinical data improve the prediction of respiratory support escalation and clinical outcomes?

Participants will:

Receive standard HFNC treatment according to clinical practice. Undergo collection of clinical, physiological, and laboratory data. Provide blood samples for metabolomic analysis during respiratory support.

研究概览

地位

招聘中

详细说明

This observational study aims to evaluate whether metabolomic signatures combined with routinely collected clinical and physiological data can improve the prediction of high-flow nasal cannula (HFNC) failure in patients with acute hypoxemic respiratory failure (AHRF). HFNC is widely used as first-line non-invasive respiratory support in AHRF; however, delayed recognition of treatment failure may lead to worse clinical outcomes, including delayed intubation and increased morbidity and mortality.

The study will prospectively enroll adult patients with AHRF treated with HFNC. Clinical variables, respiratory parameters, laboratory results, and patient outcomes will be collected during routine clinical care. Blood samples will also be obtained for metabolomic analysis to identify molecular profiles associated with HFNC success or failure.

The primary objective is to identify metabolomic and clinical predictors associated with HFNC failure and escalation of respiratory support. Secondary objectives include evaluating the association between metabolomic patterns and relevant clinical outcomes such as endotracheal intubation, duration of respiratory support, intensive care unit (ICU) length of stay, and mortality. The study also aims to develop predictive models integrating biological and clinical data to support personalized respiratory management strategies in AHRF.

研究类型

观察性的

注册 (估计的)

300

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Francisco José Parrilla-Gómez, MD, Phd
  • 电话号码:+34 747424848
  • 邮箱:fparilla@hmar.cat

研究联系人备份

  • 姓名:Joan Ramon Masclans Enviz, MD, PhD
  • 电话号码:+34 639383309
  • 邮箱:jrmasclans@hmar.cat

学习地点

    • Catalonia
      • Barcelona、Catalonia、西班牙、08003
        • 招聘中
        • Hospital Del Mar
        • 接触:
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

Adult patients admitted to intensive care units (ICUs) with acute hypoxemic respiratory failure (AHRF) requiring treatment with high-flow nasal cannula (HFNC) as part of routine clinical care. Participants will be prospectively recruited from tertiary-care hospitals in Catalonia, Spain, including: Hospital del Mar, Hospital de Bellvitge, Hospital Parc Taulí, Hospital Joan XXIII

描述

Inclusion Criteria:

  • Adult patients (≥18 years old).
  • Admission to the intensive care unit (ICU) with acute hypoxemic respiratory failure (AHRF).
  • Treatment with high-flow nasal cannula (HFNC) as the initial respiratory support strategy.
  • Inclusion within the first 24 hours after HFNC initiation.
  • Provision of informed consent by the patient or legally authorized representative.

Exclusion Criteria:

  • Age <18 years.
  • Active do-not-resuscitate (DNR) orders or limitation of therapeutic effort.
  • Refusal or inability to provide informed consent.
  • Previous invasive mechanical ventilation before study inclusion.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Adult Patients With Acute Hypoxemic Respiratory Failure Treated With HFNC
Adult patients with acute hypoxemic respiratory failure receiving high-flow nasal cannula (HFNC) as part of routine clinical care. Clinical, physiological, and metabolomic data will be collected to evaluate predictors of HFNC failure and respiratory support escalation.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
HFNC Failure
大体时间:Within the first 28 days after HFNC initiation.
Failure of high-flow nasal cannula (HFNC), defined as the need for invasive mechanical ventilation in patients with acute hypoxemic respiratory failure (AHRF).
Within the first 28 days after HFNC initiation.

次要结果测量

结果测量
措施说明
大体时间
Predictive Performance of the Metabolomic-Clinical Model
大体时间:Baseline and within the first 24 hours after HFNC initiation.
Comparison of the predictive accuracy of the metabolomic-clinical model versus the ROX index for predicting HFNC failure.
Baseline and within the first 24 hours after HFNC initiation.

其他结果措施

结果测量
措施说明
大体时间
ICU Mortality
大体时间:Up to ICU discharge or 28 days.
All-cause mortality during ICU admission.
Up to ICU discharge or 28 days.
Duration of Respiratory Support
大体时间:Up to 28 days.
Duration of HFNC therapy and invasive mechanical ventilation among patients requiring intubation.
Up to 28 days.
Association Between Metabolomic Profiles and Clinical Phenotypes
大体时间:Baseline, day 3, and day 5.
Association between metabolomic biomarkers and clinical phenotypes according to sex, age, and etiology of acute hypoxemic respiratory failure.
Baseline, day 3, and day 5.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年6月4日

初级完成 (估计的)

2029年5月1日

研究完成 (估计的)

2029年5月1日

研究注册日期

首次提交

2026年5月19日

首先提交符合 QC 标准的

2026年5月19日

首次发布 (实际的)

2026年5月26日

研究记录更新

最后更新发布 (实际的)

2026年6月8日

上次提交的符合 QC 标准的更新

2026年6月4日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • 2025/12387/I
  • PI25/00024 (其他赠款/资助编号:Instituto de Salud Carlos III)
  • 202520-30-31 (其他赠款/资助编号:Fundació La Marató de TV3)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

IPD 计划说明

Both male and female participants will be included. Sex-specific metabolomic analyses will be explored as part of the study objectives.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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