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OpenTrials
Terminated

NCT Number: NCT04193878

ARrest RESpiraTory Failure From PNEUMONIA

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.

Why the study stopped: Per DSMB's review of interim analysis, the study has reached the pre-specified futility criteria
Terminated

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University of Alabama Birmingham - Main & Highlands, Birmingham, Alabama, United States

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Who can participate

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:

  • Hospitalization for acute (defined as ≤ 14 days) onset of symptoms (cough, sputum production, or dyspnea), AND 2. Radiographic evidence of pneumonia by chest radiograph or CT scan, AND 3. One of the following:
  • Evidence of systemic inflammation (temperature < 35◦C or > 38◦C OR WBC > or < upper or lower limits for site OR procalcitonin > 0.5 mcg/L), OR
  • Known current immunosuppression preventing inflammatory response, OR
  • High clinical suspicion of pneumonia with microbiologic confirmation of infection. Microbiologic confirmation will include a positive nasal swab for a known respiratory virus; a sputum culture growing a likely pathogenic organism plus moderate or greater WBCs (not required for immunocompromised patients); or a positive blood culture with a likely pathogenic organism - e.g., ¼ vials with S. Epidermidis would NOT qualify)

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

  • Inability to randomize within 48 hours of presentation to enrolling hospital (randomization beyond 24 hours will be limited to patients with persistent hypoxemia defined by an SpO2 < 97% while on > 3L/min O2)
  • Intubation (or impending intubation) prior to enrollment

a. Patients receiving HFNC oxygen or NIV prior to enrollment are not excluded

  • A condition requiring inhaled corticosteroids or beta-agonists (patients receiving inhaled beta-agonists in the ED without an established indication will be eligible if treating clinician is willing to discontinue subsequent treatments)
  • Chronic systemic steroid therapy equivalent to >10 mg prednisone
  • COVID-19 positive patients receiving > 6 mg dexamethasone (40 mg prednisone equivalent dose) except for stress dose steroids for septic shock
  • Non-COVID-19 pneumonia patients receiving systemic steroid > 10 mg prednisone except for stress dose steroids for septic shock
  • Chronic lung or neuromuscular disease requiring daytime oxygen or mechanical ventilation other than for obstructive sleep apnea (OSA) or obesity hypoventilation syndrome
  • Not anticipated to survive > 48 hours or not expected to require > 48 hours of hospitalization
  • Contraindication or allergy to inhaled corticosteroids or beta-agonists
  • Patients with heart rate > 130 bpm, ventricular tachycardia or new supraventricular tachycardia within last 4 hours will be potentially eligible for enrollment after the condition has resolved
  • Patients with K+ < 3.0 will be potentially eligible for enrollment after the condition has resolved
  • Patient not committed to full support other than intubation or resuscitation (i.e., DNR/DNI status allowed)
  • Pregnancy
  • Incarcerated individual
  • Physician refusal of consent to protocol
  • Patient/surrogate refusal of consent to protocol

Treatment and study plan

Inhaled budesonide and formoterol

Drug

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)

Inhaled placebo

Drug

aerosolized saline (4 ml of 0.9% saline) twice daily for up to 5 days

Other names: aerosolized 0.9% saline

Primary outcomes

  1. Acute Respiratory Failure (ARF)

    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

Secondary outcomes

  1. Hospital Length of Stay

    Time frame: within 60 days of randomization (day 0)

  2. Duration of Need for Supplemental Oxygen

    Time frame: within 30 days of randomization (day 0)

  3. Proportion of Patients Intubated for Respiratory Failure

    Time frame: Within 7 days of randomization (day 0)

  4. Oxygen Failure Free Days to Day 28

    Time frame: Until Day 28

  5. Progression to Systemic Steroid Therapy for Pneumonia

    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.

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)
  • National Institutes of Health (NIH)

Registry information

Official study title

ARrest RESpiraTory Failure From PNEUMONIA (ARREST PNEUMONIA)

Acronym: ARREST

Important dates

Study start
2020
Primary completion
2025
Study completion
2025
First posted
Dec 10, 2019
Registry last updated
Aug 6, 2026

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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