Inhaled budesonide and formoterol
Drugaerosolized doses of budesonide (1.0 mg/2 ml) and formoterol (20 mg/2 ml) twice daily for up to 5 days
Other names: Pulmicort Respules (budesonide) and Perforomist (formoterol)
NCT Number: NCT04193878
This research study seeks to establish the effectiveness of a combination of an inhaled corticosteroid and a beta agonist compared to placebo for the prevention of acute respiratory failure (ARF) in hospitalized patients with pneumonia and hypoxemia.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
University of Alabama Birmingham - Main & Highlands, Birmingham, Alabama, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients 18 years or older with
Severe pneumonia defined as:
AND Hypoxemia defined as new requirement for daytime supplemental oxygen with SpO2 < 92% on room air, ≤ 96% on ≥ 2 L/min oxygen, or > 6L/min or non-invasive ventilation regardless of SpO2 at enrollment. Patients admitted with pneumonia but not meeting criteria for hypoxemia will be followed for up to 48 hours from ED admission to enrolling hospital to assess for development of qualifying hypoxemia.
Exclusion criteria
a. Patients receiving HFNC oxygen or NIV prior to enrollment are not excluded
aerosolized doses of budesonide (1.0 mg/2 ml) and formoterol (20 mg/2 ml) twice daily for up to 5 days
Other names: Pulmicort Respules (budesonide) and Perforomist (formoterol)
aerosolized saline (4 ml of 0.9% saline) twice daily for up to 5 days
Other names: aerosolized 0.9% saline
Time frame: within 7 days of randomization (day 0)
High flow nasal cannula (HFNC >=20L/mon O2) and/or Noninvasive ventilation (NIV) use for greater than 36 hours OR Invasive mechanical ventilation for greater than 36 hours OR Death in a patient placed on respiratory support (HFNC, NIV, ventilator) who dies before 36 hours
Time frame: within 60 days of randomization (day 0)
Time frame: within 30 days of randomization (day 0)
Time frame: Within 7 days of randomization (day 0)
Time frame: Until Day 28
Time frame: Within 7 days of randomization (day 0)
Progression defined as initiating post-randomization, open-label steroids if not already receiving dexamethasone for COVID at baseline.
Stanford University
Other
ARrest RESpiraTory Failure From PNEUMONIA (ARREST PNEUMONIA)
Acronym: ARREST
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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