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High Flow Tracheal Oxygen for Weaning of Tracheostomized Patients (HFTO-WEAN)

29. mai 2026 oppdatert av: Zainab Alduhailib, King Faisal Specialist Hospital & Research Center

High Flow Tracheal Oxygen for Weaning of Tracheostomized Mechanically Ventilated Patients: A Pilot Randomised Controlled Trial (HFTO WEAN Trial)

In this pilot randomized controlled trial (RCT), the investigators aim to explore the feasibility of conducting a powered RCT that examines the efficacy and safety of high flow tracheal oxygen (HFTO) in weaning critically ill tracheostomy patients from mechanical ventilation.

Objective of the study

  1. To assess the feasibility of conducting a larger RCT as primary objective.
  2. To explore the effect of using HFTO in mechanically ventilated tracheostomized critically ill patients on ventilator-free days (VFD) compared to standard of care method using tracheal mask (TM) as secondary objective.

Studieoversikt

Detaljert beskrivelse

Background High Flow Nasal Cannula (HFNC) use has increased over the past decade in critically ill patients with acute hypoxic respiratory failure. HFNC involves the delivery of oxygen at a higher flow reaching up to 60 L/min, which is heated and humidified to enhance tolerability of the device. HFNC improves oxygenation and decrease work of breathing through several mechanisms including: (1) improving high oxygen delivery through decrease in the inspired fraction of inspired oxygen (FiO2) dilution, (2) decreasing the patient's work of breathing through matching of the patient's needed flow and the minimal amount of positive end-expiratory pressure (PEEP) exerted on the upper airway and alveoli caused by the constant flow, which could help in alveoli recruitment and improvement in oxygenation (up to 5 cm of end-expiratory pressure), (3) anatomical dead space washout leading to washout of carbon dioxide (CO2) and thus decreases the work of breathing by the continuous flow to the pharynx and upper part of the trachea.

Evidence on HFNC in critically ill patients Several randomized controlled trials (RCT) have assessed the role of HFNC in critically ill patients for different indications. In a systematic review of 9 RCTs, HFNC compared to conventional oxygen therapy, reduced the need for intubation (relative risk [RR] 0.85, 95% confidence interval [CI] 0.74-0.99, low certainty) or escalation of oxygen therapy to non-invasive positive pressure ventilation (NIPPV) (RR 0.71, 95% CI 0.51-0.98, low certainty) for patients with acute hypoxic respiratory failure without an increase in mortality. In addition, compared to NIPPV in acute hypoxic respiratory failure, HFNC showed similar risk for intubation (RR, 0.93; 95% CI 0.69-1.27, low certainty) without survival benefit. These results prompted a strong recommendation (moderate certainty) for the use of HFNC over conventional oxygen therapy in acute hypoxic respiratory failure from the European Society of Intensive Care Medicine. The use of HFNC was expanded to the peri-extubation period for patients at high-risk of extubation failure [5]. The high-risk population was defined as: age > 65, congestive heart failure, moderate-severe chronic obstructive pulmonary disease (COPD), APACHE II score > 12, body mass index > 30 Kg/m2, airway patency or secretion problems, difficulty weaning, ≥2 comorbidities, or duration of invasive mechanical ventilation >7 days. Evidence from four RCTs showed that HFNC use post-extubation reduced the need for intubation when compared to conventional oxygen therapy (RR 0.46, 95% CI 0.30-0.70), and it resulted in little to no difference in intubation rates when compared to NIPPV (RR 1.16, 95% CI 0.86-1.57). The utilization of HFNC for hypoxic respiratory failure has been extensively studied, but not for hypercapnic respiratory failure. Few observational studies and RCTs assessed the safety of HFNC in hypercapnic respiratory failure. When comparing HFNC to NIPPV for patients with hypercapnic respiratory failure, a systematic review of five RCTs showed no difference in intubation rates (odds ratio [OR]= 0.92, 95% CI 0.45-1.88) and mortality (OR 1.33, 95% CI 0.68-2.60). Similar results were obtained for patients with COPD. However, the evidence is limited by imprecision and heterogeneity and a conclusion about the safety of such an approach needs to be studied further.

Evidence of high-flow tracheal oxygen (HFTO) in tracheostomized patients Recently, HFTO has been used for weaning mechanical ventilation in tracheostomy patients at high risk of weaning failure. In a single-arm cross-over study, 14 mechanically ventilated patients through tracheostomy with prolonged weaning after more than 7 days from the first separation attempt according to Weaning according to a New Definition (WIND) study criteria were enrolled [16]. After a successful spontaneous breathing trial (SBT), the patients were placed on HFTO for 2 hours interrupted by 1-hour of conventional oxygen therapy through T-Piece to assess the physiological effect of HFTO. The study showed a lack of HFTO effect on the neuro-respiratory drive using electrical diaphragmatic activity measurement, work of breathing, and the ratio of peripheral arterial oxygen saturation to the inspired fraction of oxygen (PaO2:FiO2) ratio in comparison to conventional oxygen therapy. This study might suggest that HFTO works differently from HFNC. In contrast, another study of 26 tracheostomized patients who were weaned from mechanical ventilation and spontaneously breathing on conventional oxygen therapy for at least 24 hours, were randomly placed on different gas flow rates through HFTO for 30 minutes (10L /min, 30 L/min, or 50 L/min) with no washout period [17]. Compared to conventional oxygen therapy, HFTO improved the PaO2:FiO2 ratio but the CO2 remained stable. In addition, HFTO slightly reduced the respiratory rate and the negative swings in airway pressures during inspiration, and increase the mean and peak expiratory pressures at flows of 50 L/min. At a lower flow of 30 L/min, conventional oxygen therapy was similar to HFTO with regard to oxygenation and tracheal pressure. Of interest, although there was an increment in the measured tracheal expiratory pressure, it was lower than the pressures measured during HFNC. This could be explained by the limited resistance in tracheostomized patients in comparison to HFNC where the upper airway creates resistance and a higher expiratory pressure. A crossover RCT (n=20), in which tracheostomized patients were randomized to either HFTO at 50 L/min or T-piece and data was collected at 5 minutes and 15 minutes of each intervention. At 15 minutes, the patients on HFTO showed higher ratio of peripheral arterial oxygen saturation to the inspired fraction of oxygen (SPO2: FiO2) ratio and mean airway pressures with lower FiO2 requirements. However, respiratory rate and CO2 remained the same. Recently, a few case reports were also published about the utilization of HFTO for successful weaning, which showed that higher positive mean airway and tracheal pressures, improved PaO2: FiO2 ratio, and reduced inspiratory effort. Furthermore, a recent RCT (n=330) of tracheostomized critically ill patients who were weaned from mechanical ventilation and deemed ready for decannulation were randomized to either continuous HFTO with tracheostomy capping or capping with intermittent HFTO for 24 hours. Continuous HFTO utilization during the capping procedure was associated with shorter time to decannulation (median 6 [interquartile range (IQR) 5-7] days vs. 13 [IQR, 11-14] days) without decannulation failure.

Knowledge gap and aims of this study The evidence on the efficacy of using HFTO in patients with tracheostomy is limited. Such an approach might be costly due to the use of HFTO set and the need for a special interface to fit the HFTO through tracheostomy. If the use of HFTO proves to a safe and advantageous strategy, then the timing, population, dose, and average duration of weaning need to be addressed in controlled trials. In this pilot RCT, the investigators aim to explore the feasibility of conducting a powered RCT that examines the efficacy and safety of HFTO in weaning critically ill tracheostomy patients from mechanical ventilation.

Studietype

Intervensjonell

Registrering (Antatt)

88

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

  • Navn: Zainab Al Duhailib, MBBS, MSc, EDIC
  • Telefonnummer: 42817 00966112162919
  • E-post: zainajd@gmail.com

Studer Kontakt Backup

Studiesteder

      • Riyadh, Saudi-Arabia
        • Rekruttering
        • King Faisal Specialist Hospital and Research Centre
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  1. Adults ≥ 18 years of age
  2. Intensive care unit (ICU) patients with tracheostomy inserted during the index ICU admission.
  3. Mechanically ventilated for ≤60 days.
  4. Successful spontaneous breathing trial for 1 hour.

Exclusion Criteria:

  1. Planned tracheostomy post head and neck surgery with ICU stay less than 48 hours
  2. Patient transferred from another hospital only if the intubation and tracheostomy dates are unavailable, otherwise would be eligible.
  3. Patient with an imminent plan for palliation and comfort care.
  4. Patient or substitute decision-maker declines consent to the study.
  5. The treating physician declines consent to the study.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Standard of care
Standard of care method using tracheal mask (TM) for weaning tracheostomized mechanically ventilated patients
Standard of care using tracheal mask (TM) oxygen for weaning tracheostomized mechanically ventilated patients
Andre navn:
  • tracheal mask
Eksperimentell: Intervention arm
High-flow tracheal oxygen therapy (HFTO) for weaning tracheostomized mechanically ventilated patients
High-flow tracheal oxygen for weaning tracheosstomized mechanically ventilated patients
Andre navn:
  • HFTO

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Consent Rate
Tidsramme: 1 Year

A successful consent rate will be defined as ≥70% of SDMs or patients approached to consent, agreeing to participate in the trial.

This will be calculated as the proportion of substitute decision makers (SDMs) or patients who consent to participate out of those approached.

1 Year
Recruitment Rate
Tidsramme: 1 Year

A successful recruitment rate will be defined as achieving our target enrolment of 88 patients or recruiting at least 2 patients per month throughout the duration of the trial.

The number of patients recruited per month will be tracked to ensure the target of 2 patients per month is met.

1 Year
Protocol Adherence
Tidsramme: 1 Year

A successful adherence will be defined as ≥ 75% of patients receiving HFTO in the intervention arm and ≥ 75% of patients receiving TM in the control arm (crossover in the control arm <25%).

This would be calculated as the proportion of patients assigned to the intervention arm that received HFTO, and the proportion of those patients assigned to the control arm receiving TM.

1 Year

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Ventilator-free days (VFDs) at day-30 from enrollment.
Tidsramme: 30 days from enrollment
The number of days free from mechanical ventilation within the first 30 days post-enrollment will be recorded.
30 days from enrollment
Successful liberation from mechanical ventilation at 30-days from enrollment
Tidsramme: 30 days from enrollment
Defined as spontaneous ventilation through tracheostomy without any mechanical ventilation during 7 consecutive days or discharged with spontaneous breathing, whichever comes first
30 days from enrollment
Mortality at 30 days.
Tidsramme: 30 days from enrollment
30 days from enrollment
ICU length of stay at 30-days.
Tidsramme: 30 days from enrollment
30 days from enrollment
Hospital length of stay at 30-days.
Tidsramme: 30 days from enrollment
30 days from enrollment
Discharge on mechanical ventilation at 30 days (home, long-term facility, another hospital).
Tidsramme: 30 days from enrollment
30 days from enrollment
Physiological outcomes (Vital Signs Measurements)
Tidsramme: 7 days from enrollment
The difference between respiratory rate (measured as breaths per minute), heart rate (measured as beats per minute) before and 1-2 hours after the intervention or control in the first 7 days in both groups.
7 days from enrollment
Physiological outcomes (Oxygenation and Ventilation Measurements from Arterial Blood Gas)
Tidsramme: 7 days from enrollment
The difference between pH, PaCo2: partial pressure of arterial carbon dioxide (measured in kPa), PaO2: partial pressure of oxygen in arterial blood gas (measured in kPa), SaO2: arterial oxygen saturation (measured as %), FiO2 (measured as %), and PaO2:FiO2: the ratio of arterial oxygen partial pressure to the fractional inspired oxygen (measured in mmHg) before and 1-2 hours after the intervention or control in the first 7 days in both groups.
7 days from enrollment
Physiological outcomes (Oxygenation Parameters from Vital Signs)
Tidsramme: 7 days from enrollment
The difference between SpO2:FiO2: the ratio of oxygen saturation from pulse oximetry to the fraction of inspired oxygen before and 1-2 hours after the intervention or control in the first 7 days in both groups.
7 days from enrollment

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Zainab Al Duhailib, MBBS, MSc, EDIC, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

17. mai 2026

Primær fullføring (Antatt)

1. mai 2027

Studiet fullført (Antatt)

1. mai 2027

Datoer for studieregistrering

Først innsendt

7. april 2026

Først innsendt som oppfylte QC-kriteriene

24. april 2026

Først lagt ut (Faktiske)

30. april 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

2. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

29. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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