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Methylprednisolone for Patients With COVID-19 Severe Acute Respiratory Syndrome (MP-C19)

U

University of Trieste

Status

Completed

Conditions

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

Treatments

Drug: Methylprednisolone
Other: standard care

Study type

Observational

Funder types

Other

Identifiers

NCT04323592
MP-19 023_2020

Details and patient eligibility

About

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).

Full 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.

Enrollment

173 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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

Trial design

173 participants in 2 patient groups

Exposed to Methylprednisolone
Description:
Consecutive SARS-CoV-2 positive patients with severe acute respiratory syndrome treated with methylprednisolone (MP) at low prolonged dose, fulfilling inclusion and exclusion criteria.
Treatment:
Other: standard care
Drug: Methylprednisolone
Non-exposed to Methylprednisolone
Description:
Concurrent patients fulfilling the same inclusion and exclusion criteria, never treated with steroids.
Treatment:
Other: standard care

Trial documents
3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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