Efficacy of DEXamethasone in Patients With Acute Hypoxemic REspiratory Failure Caused by INfEctions

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorDr. Negrin University Hospital

About this trial

Background: There are no proven therapies specific for pulmonary dysfunction in patients with acute hypoxemic respiratory failure (AHRF) caused by infections (including Covid-19). The full spectrum of AHRF ranges from mild respiratory tract illness to severe pneumonia, acute respiratory distress syndrome (ARDS), multiorgan failure, and death. The efficacy of corticosteroids in AHRF and ARDS caused by infections remains controversial.

Methods: This is a multicenter, randomized, controlled, open-label clinical trial testing dexamethasone in mechanically ventilated adult patients with established AHRF (including ARDS) caused by confirmed pulmonary or systemic infections, admitted in a network of Spanish ICUs. Eligible patients will be randomly assigned to receive dexamethasone: either 6 mg/d x 10 days or 20 mg/d x 5 days followed by 10 mg/d x 5 days. The primary outcome is 60-day mortality. The secondary outcome is the number of ventilator-free days at 28 days. All analyses will be done according to the intention-to-treat principle.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

age 18 years or older;

intubated and mechanically ventilated;

acute onset of AHRF (as defined by a PaO2/FiO2 ≤300 mmHg during at least 6 hours from diagnosis. For the measurement of PaO2 and calculation of PaO2/FiO2 ratio, the minimum accepted value for PEEP is 5 cmH2O and for FiO2 is 0.3. ARDS is defined by Berlin criteria,4 which includes: (i) having pneumonia or worsening respiratory symptoms, (ii) bilateral pulmonary infiltrates on chest imaging (x-ray or CT scan), (iii) absence of left atrial hypertension or no clinical signs of left heart failure, and (iv) hypoxemia, as defined by a PaO2/FiO2 ≤300 mmHg on positive end-expiratory pressure (PEEP) of ≥5 cmH2O, regardless of FiO2.

Pulmonary or systemic infectious etiology of AHRF.

Disqualifiers

Patients with a known contraindication to corticosteroids,

Patient included in another therapeutic clinical trial

Lack of informed consent

Trial design

Design model

Parallel

Treatments tested in this trial

  • Dexamethasone

    Drug

    Intravenous dexamethasone (low vs. moderate doses) during 10 days

Treatment groups

980 Participants
are divided into 2 treatment groups
Group A: Dexamethasone (low dose)Active comparator 1 intervention
Group B: Dexamethasone (moderate dose)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

60-day mortality

All-cause mortality at 60 days after randomization

Time frame
60 days

Secondary outcomes

1

Ventilator-free days

Number of ventilator-free days (VFDs) at Day 28 (defined as days being alive and free from mechanical ventilation at day 28 after randomization. For patients ventilated 28 days or longer and for subjects who die, VFD is 0.

Time frame
28 days

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Dr. Negrin University Hospital

Lead sponsor

Li Ka Shing Knowledge Institute

Collaborator

Consorcio Centro de Investigación Biomédica en Red (CIBER)

Collaborator