The Severe Acute Respiratory Syndrome COronaVirus 2 (SARS-CoV2) is a new and recognized infectious disease of the respiratory tract. Most cases are mild or asymptomatic. However, around 5% of all patients develop Acute Respiratory Distress Syndrome (ARDS), which is the leading mortality cause in these patients. Corticosteroids have been tested in deferent scenarios of ARDS, including viral pneumonia, and the early use of dexamethasone is safe and appears to reduce the duration of mechanical ventilation in ARDS patients. Nevertheless, no large, randomized, controlled trial was performed evaluating the role of corticosteroids in patients with ARDS due SARS-CoV2 virus. Therefore, the present study will evaluate the effectiveness of dexamethasone compared to control (no corticosteroids) in patients with moderate and severe ARDS due to SARS-CoV2 virus.
The Severe Acute Respiratory Syndrome COronaVirus 2 (SARS-CoV2) is a new and recognized infectious disease of the respiratory tract, and its outbreak deemed a pandemic in early March 2020. Estimates show around 5% of all patients develop Acute Respiratory Distress Syndrome (ARDS), which due to its severity, consumes most Intensive Care Units (ICU) resources and is the leading mortality cause in this population. Given its burden, therapies that reduce the duration of mechanical ventilation or decrease the morbimortality are needed. Studies indicate that inflammation and cytokine storm might be involved in the pathophysiological pathway to ARDS in these patients. Corticosteroids have been tested in deferent scenarios of ARDS, including viral pneumonia, and the early use of dexamethasone is safe and appears to reduce the duration of mechanical ventilation in ARDS patients. A recent small retrospective study evaluating the role of corticosteroids found no association between corticosteroids and hospital length of stay, virus clearance, and symptoms' duration. However, the retrospective nature of data, small sample size (31 patients), and no protocol for corticosteroids administration undermine its results. Therefore, the present study will evaluate the effectiveness of dexamethasone compared to control (no corticosteroids) in ventilator-free days at 28 days in patients with moderate and severe ARDS due to SARS-CoV2 virus in Brazil.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
299
Dexamethasone administration for 10 consecutive days after randomization.
Fundação Social Rural de Colatina
Colatina, Esoírito Santo, Brazil
Hospital Ana Nery
Salvador, Estado de Bahia, Brazil
Instituto de Cardiologia do Distrito Federal
Brasília, Federal District, Brazil
Hospital Vera Cruz AS
Belo Horizonte, Minas Gerais, Brazil
Hospital Maternidade E Pronto Socorro Santa Lucia Ltda
Poços de Caldas, Minas Gerais, Brazil
Universidade Estadual de Londrina
Londrina, Paraná, Brazil
Eurolatino Natal Pesquisas Médicas Ltda
Natal, Rio Grande do Norte, Brazil
Irmandade da Santa Casa de Misericordia de Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil
Maestri E Kormann Consultoria Medico-Cientifica
Blumenau, Santa Catarina, Brazil
Sociedade Literaria e Caritativa Santo Agostinho
Criciúma, Santa Catarina, Brazil
...and 11 more locations
Ventilator-free days
Ventilator-free days, defined as alive and free from mechanical ventilation, at 28 days after randomization.
Time frame: 28 days after randomization
Evaluation of the clinical status
Evaluation of the clinical status of patients on the 15th day after randomization defined by the 6-point Ordinal Scale, this scale ranges from 1 (Not hospitalized) to 6 (Death) with higher scores meaning worse outcomes.
Time frame: 15 days after randomization
All-cause mortality
All-cause mortality rates at 28 days after randomization.
Time frame: 28 days after randomization
Mechanical ventilation duration
Number of days of mechanical ventilation from randomization to day 28.
Time frame: 28 days after randomization
Sequential Organ Failure Assessment (SOFA) Score
Sequential Organ Failure Assessment (SOFA) Score 48 hours, 72 hours and 7 days after randomization
Time frame: Score at 48 hours, 72 hours and 7 days after randomization
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