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Active, not recruiting Observational

Weaning From High Flow Nasal Oxygen in Acute Respiratory Failure : a Target Trial Emulation

NCT07030413 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2019-11-01
Last updated
2025-08-08

Condition(s) studied

Respiratory Failure With HypoxiaRespiratory Failure, ICUHigh-Flow Nasal Oxygen Therapy

Study summary

Acute respiratory failure is a frequent reason for admission to the intensive care unit (ICU). It is associated with high healthcare consumption and mortality.

High-flow nasal oxygen (HFNO) improves comfort, reduces the risk of intubation and may reduce the risk of mortality in the most severe patients with acute hypoxemic respiratory failure compared with other oxygenation strategies. Therefore, HFNO is recommended as a first-line non-invasive oxygenation strategy in acute hypoxemic respiratory failure.

The timing of weaning patients from HFNO is complex. On the one hand, failure to wean from HFNO is associated with prolonged duration of HFNO and prolonged ICU stay. On the other hand, continued HFNO in patients ready to be weaned may unnecessarily prolong ICU stay and contribute to overwhelming of ICU capacities.

The overarching goal of this study is to identify the characteristics of patients in whom weaning from HFNO is not beneficial.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult patients (age \> 18) * Admitted to participating ICUs * Treated with HFNO at the attending physician's discretion for acute respiratory failure (defined as respiratory rate ≥ 25 breaths/min) Exclusion Criteria: * Prophylactic HFNO to prevent reintubation after extubation * Noninvasive ventilation before HFNO initiation

Primary outcome measure(s)

  • Hospital-free days at day 90 — 90 days
    The number of days alive out of hospital between pseudorandomization and D90. For patients who died, the hospital-free days at day 90 will be equal to 0.

Trial sites (3)

FacilityCityRegionStatus
University Hospital Bordeaux Bordeaux France
University Hospital Limoges Limoges France
University Hospital Poitiers Poitiers France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07030413 on ClinicalTrials.gov ↗ ← All trials in France