Hydrocortisone for COVID-19 and Severe Hypoxia

Scandinavian Critical Care Trials Group30 enrolled

Overview

We aim to assess the benefits and harms of low-dose hydrocortisone in patients with COVID-19 and severe hypoxia.

Background: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has caused a pandemic of coronavirus disease (COVID-19) with many patients developing severe hypoxic respiratory failure. Many patients have died, and healthcare systems in several countries have been or will be overwhelmed because of a surge of patients needing hospitalisation and intensive care. There is no proven treatment for COVID-19; the care is supportive, including respiratory and circulatory support. For other patient groups with similar critical illness (acute respiratory disease syndrome and septic shock), corticosteroids are used because they reduce the duration of mechanical ventilation, length of stay in the intensive care unit, and potentially also mortality. Corticosteroids have been used in some patients with COVID-19, but the recommendations in clinical guidelines differ; some suggest their use, others against. Objectives: We aim to assess the effects of low-dose intravenous hydrocortisone on the number of days alive without life-support in adult patients with COVID-19 and severe hypoxia. Design: Multicentre, parallel-group, centrally randomised, stratified, blinded, clinical trial. Population: Adult patients with documented COVID-19 receiving at least 10 L/min of oxygen independent of delivery system OR mechanical ventilation. Experimental intervention: Continuous IV infusion of hydrocortisone 200 mg daily will be given for 7 days in addition to standard care. Control intervention: Continuous IV infusion of matching placebo (0.9% saline) will be given in addition to standard care (no corticosteroids). Outcomes: The primary outcome is days alive without life support (i.e. mechanical ventilation, circulatory support, or renal replacement therapy) at day 28. Secondary outcomes are serious adverse reactions (i.e. anaphylactic reaction to hydrocortisone, new episode of septic shock, invasive fungal infection or clinically important gastrointestinal bleeding); days alive without life support at day 90; days alive and out of hospital at day 90; all-cause mortality at day 28, day 90 and 1 year; and health-related quality of life at 1 year. Sample size: A total of 1000 participants will be randomised in order to detect a 15% relative reduction in 28-day mortality combined with a 10% reduction in time on life support among the survivors with a power of 85%.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Covid-19 Hypoxia

Interventions

HydrocortisoneDRUG

Continuous infusion: 200 mg (104 ml) every 24 hours, Bolus injections: 50 mg (10 ml) every 6 hours, Total treatment duration: 7 days

Sodium Chloride 9mg/mLDRUG

Continuous infusion: 104 ml every 24 hours, Bolus injections: 10 ml every 6 hours, Total treatment duration: 7 days

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: All the following criteria must be fulfilled: * Aged 18 years or above AND * Confirmed SARS-CoV-2 (COVID-19) requiring hospitalisation AND * Use of one of the following: * Invasive mechanical ventilation OR * Non-invasive ventilation or continuous use of continuous positive airway pressure (CPAP) for hypoxia OR * Oxygen supplementation with an oxygen flow of at least 10 L/min independent of delivery system Exclusion Criteria: We will exclude patients who fulfil any of the following criteria: * Use of systemic corticosteroids for any other indication than COVID-19 * Invasive mechanical ventilation for more than 48 hours * Invasive fungal infection * Fertile woman (\< 60 years of age) with positive urine human gonadotropin (hCG) or plasma-hCG * Known hypersensitivity to hydrocortisone * A patient for whom the clinical team has decided not to use invasive mechanical ventilation * Previously randomised into the COVID STEROID trial * Informed consent not obtainable

Locations (14)

Aarhus University Hospital - Dept of Intensive care

Aarhus, Denmark

Rigshospitalet

Copenhagen, Denmark

Dept of Infectious diseases, Rigshospitalet

Copenhagen, Denmark

Outcomes

Primary Outcomes

Days alive without life support at day 28

Days alive without life support (i.e. invasive mechanical ventilation, circulatory support or renal replacement therapy) from randomisation to day 28

Time frame: Day 28 after randomisation

Secondary Outcomes

All-cause mortality at day 28

Death from all causes

Time frame: Day 28 after randomisation

Days alive without life support at day 90

Days alive without life support (i.e. invasive mechanical ventilation, circulatory support or renal replacement therapy) from randomisation to day 90

Time frame: Day 90 after randomisation

All-cause mortality at day 90

Death from all causes

Time frame: Day 90 after randomisation

Number of participants with one or more serious adverse reactions

Defined as new episodes of septic shock, invasive fungal infection, clinically important GI bleeding or anaphylactic reaction

Time frame: Day 14 after randomisation

Days alive and out of hospital at day 90

Number of days alive and out of hospital not limited to the index admission

Time frame: Day 90 after randomisation

All-cause mortality at 1 year after randomisation

Death from all causes

Time frame: 1 year after randomisation

Health-related quality of life at 1 year

Data from ClinicalTrials.gov

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