Official Title
Prolonged Low Doses of Methylprednisolone for Patients With COVID-19 Severe Acute Respiratory Syndrome
Brief Summary

COVID-19 infection is overwhelming Italian healthcare. There is an urgent need for a solution to the lack of ICU beds and increasing deaths day after day. A recent retrospective Chinese paper (JAMA Intern Med, online March 13, 2020) showed impressive positive effect of methylprednisolone (MP) on survival of SARS-CoV-2 critically ill patients. Moreover, the Italian Infectious Disease leading institution guidelines for COVID-19 clinical management included as an option for patients with "incipient worsening of respiratory functions" methylprednisolone treatment at an approximate dose of 80mg. The main objective of this multi-centre observational trial is to analyse the association of low dose prolonged infusion of methylprednisolone (MP) for patients with severe acute respiratory syndrome with composite primary end-point (ICU referral, need for intubation, in-hospital death at day 28).

Detailed Description

Comparison of two groups of patients SARS-CoV-2 positive with severe acute respiratory
syndrome:

1. Exposed to low prolonged doses of Methylprednisolone

2. Not exposed to corticosteroids (standard of care alone)

The two group will be weighted by means of a propensity score according to:

1. Sex

2. Age

3. C-reactive protein (CRP) at baseline

4. Sequential Organ Failure Assessment (SOFA) score at baseline

5. PaO2/FiO2 ratio at baseline (ratio of arterial oxygen partial pressure to fractional
inspired oxygen)

Anti-viral agents, chloroquine, respiratory support (any), and antibiotics (any) are allowed
in each study group. Corticosteroids use, other than per-protocol Methylprednisolone in the
exposed group is a reason for dropout.

1. The exposed group is treated with Methylprednisolone at study entry (baseline) according
to a protocol based on the Italian national recommendations for COVID-19 management: a
loading dose of 80 mg IV, followed by an infusion of 80 mg/day in 240 mL normal saline
at 10 mL/h. The infusion is continued for at least eight days and until achieving either
a PaO2:FiO2 > 350 mmHg or a CRP < 20 mg/L. Treatment is then switched to oral
administration of Methylprednisolone 16 mg or 20 mg IV twice daily until CRP returns to
< 20% of normal range and/or PaO2:FiO2 > 400 or SatHbO2 ≥ 95%. The decision to apply the
protocol to Covid-19 is left to the discretion of the treating team for each individual
patient.

2. Unexposed patients will be selected from concurrent consecutive COVID-19 patients with
the same inclusion and exclusion criteria and blinded to outcome data.

Completed
Severe Acute Respiratory Syndrome (SARS) Pneumonia
Coronavirus Infections
ARDS, Human

Drug: Methylprednisolone

Usual standard of care plus Methylprednisolone (MP) 80 mg/kg IV bolus, followed by MP infusion of 80 mg/day in 240 mL normal saline at 10 mL/h. The infusion is continued for at least eight days and until achieving either a PaO2:FiO2 > 350 mmHg or a CRP < 20 mg/L. Treatment is then switched to oral administration of Methylprednisolone 16 mg or 20 mg IV twice daily until CRP returns to < 20% of normal range and/or PaO2:FiO2 > 400 or SatHbO2 ≥ 95%. The decision to apply the protocol to Covid-19 is left to the discretion of the treating team for each individual patient.

Other: standard care

usual standard of care:
oxygen therapy (regular or high-flow) and monitoring
empiric antibiotic therapy
mechanical ventilation (invasive or noninvasive)
ECMO when needed and available
pronation when possible
other treatment which can be used are: antivirals, chloroquine, vitamins

Eligibility Criteria

Inclusion Criteria:

1. SARS-CoV-2 positive

2. Age >17 years and < 80 years

3. P/F < 250 mmHg

4. Bilateral pneumonia (infiltrates/interstitial)

5. CRP >10mg/dL (or >100mg/L)

6. Alternatively to 4-5-6 criteria a diagnosis of ARDS according to the Berlin definition
(Ranieri M, et al. JAMA 2012)

Exclusion Criteria:

- Heart failure as predominant cause of acute respiratory failure

- Decompensated liver cirrhosis

- Cancer

- Organ transplantation

- HIV+

- dialysis

- long-term oxygen therapy, home mechanical ventilation

- Idiopathic pulmonary fibrosis

- Progressive neuromuscular disorders (e.g. Duchenne, Pompe, ALS)

- Dementia or decompensated psychiatric diseases

- immunosuppressive treatments

- Chronic use of corticosteroids

- Use of Tocilizumab

- pregnancy

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 80 Years
Countries
Italy
Locations

Marco Confalonieri
Trieste, TS, Italy

Marco Confalonieri, MD, Principal Investigator
University of Trieste

University of Trieste
NCT Number
Keywords
SARS-CoV-2,
sars
ARDS
Methylprednisolone
MeSH Terms
Coronavirus Infections
Severe Acute Respiratory Syndrome
Respiratory Distress Syndrome
Syndrome
Methylprednisolone
Methylprednisolone Acetate
Methylprednisolone Hemisuccinate
Prednisolone
Prednisolone acetate
Prednisolone hemisuccinate
Prednisolone phosphate