Gemelli
Rome, Italy
Location status: Recruiting
NCT Number: NCT05089695
Multicenter, open label, three-arm randomized trial to assess the effect of helmet noninvasive ventilation vs. helmet continuous positive airway pressure vs. high-flow nasal oxygen on the rate of endotracheal intubation of patients with acute moderate-to-severe hypoxemic respiratory failure
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Request Info18 year and older
All sexes
Interventional
Not applicable
Rome, Italy
Location status: Recruiting
The optimal initial management of acute hypoxemic respiratory failure is uncertain. Helmet noninvasive ventilation and high-flow nasal oxygen appear as the most promising techniques in this setting. Recently, the first head-to-head randomized trial compared first-line continuous treatment with helmet pressure support ventilation with specific settings (PEEP=12 cmH2O pressure and pressure support=10-12 cmH2O) vs. high-flow nasal oxygen alone in patients with moderate-to-severe hypoxemic respiratory failure. Results showed no significant inter-group difference in the days free of respiratory support at 28 days, but lower intubation rate and increased 28-day invasive ventilation-free days in the helmet group. Use of helmet noninvasive ventilation is less frequent than use of helmet continuous positive airway pressure, which is simpler to use.
The investigators designed an open-label, multicentre randomized trial to assess the effect of helmet pressure support ventilation and continuous airway pressure as compared to high-flow nasal oxygen on the intubation rate of patients with moderate-to-severe hypoxemic respiratory failure in the intensive care unit.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients that have already received NIV, CPAP continuously for more than 24 hours before the screening visit will be excluded.
Other Exclusion Criteria:
Treatment of acute hypoxemic respiratory failure
Time frame: 28 days
The proportion of patients requiring endotracheal intubation according to predefined criteria
Time frame: 28 days
The number of days in which patients do not receive mechanical ventilation within 28 days from randomization
Time frame: 60 days
The number of days in which patients do not receive mechanical ventilation within 60 days from randomization
Time frame: 90 days
The number of days in which patients do not receive mechanical ventilation within 60 days from randomization
Time frame: 90 days
All-cause mortality, assessed at the discharge from the intensive care unit
Time frame: 90 days
All-cause mortality, assessed at the discharge from the hospital
Time frame: 90 days
All-cause 90-day mortality
Time frame: 90 days
The days not spent in the intensive care unit by the patient on a 90-day basis
Time frame: 90 days
The days not spent in the hospital by the patient on a 90-day basis
Time frame: 90 days
Incidence of pneumonia, diagnosed after the treatment start and during the ICU stay
Time frame: 90 days
Incidence of shock, diagnosed after treatment start and during the ICU stay
Time frame: 90 days
Incidence of barotrauma, defined as pneumothorax o pneumomediastinum after treatment start and during the ICU stay
Time frame: 28 days
Among patients meeting the primary endpoint, the cause of noninvasive treatment failure (as defined by the predefined intubation criteria)
Time frame: 28 days
In patients meeting the primary endpoint, the time (hours) from randomization to intubation
Contact information is provided by the study sponsor or research team.
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Other
Helmet Noninvasive Ventilation vs. Continuous Positive Airway Pressure vs. High-flow Nasal Oxygen as First-line Treatment of Acute Hypoxemic Respiratory Failure (HENIVOT2). An Open-label, Multicentre Randomized Trial
Acronym: HENIVOT2
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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