MedPath

Higher vs. Lower Doses of Dexamethasone for COVID-19 and Severe Hypoxia

Phase 3
Completed
Conditions
Hypoxia
Covid19
Interventions
Registration Number
NCT04509973
Lead Sponsor
Scandinavian Critical Care Trials Group
Brief Summary

We aim to assess the benefits and harms of higher (12 mg) vs lower doses (6 mg) of dexamethasone on patient-centered outcomes in patients with COVID-19 and severe hypoxia.

Detailed Description

Background: Preliminary results from the Randomised Evaluation of COVid-19 thERapY (RECOVERY) trial have reported a reduction in 28-day mortality with low-dose dexamethasone (6 mg) once daily versus no intervention in hospitalised patients with COVID-19; an effect that may have been more pronounced in patients with increasing hypoxia. Yet, higher doses of dexamethasone may be beneficial in patients with non-COVID-19 acute respiratory distress syndrome. At present, it is unclear what dose of dexamethasone is most beneficial in patients with COVID-19 and severe hypoxia, and clinical equipoise exists.

Objective: We aim to assess the effects of higher (12 mg) vs lower doses (6 mg) of intravenous dexamethasone on the number of days alive without life-support in adult patients with COVID-19 and severe hypoxia.

Design: International, 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: Dexamethasone 12 mg once daily for up to 10 days in addition to standard care.

Control intervention: Dexamethasone 6 mg once daily for up to 10 days in addition to standard care.

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) at day 28; days alive without life support at day 90; days alive and out of hospital at day 90; all-cause mortality at day 28, 90 and 180; and health-related quality of life at day 180.

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%.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1000
Inclusion Criteria

All of the following 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
Read More
Exclusion Criteria

We will exclude patients who fulfil any of the following criteria:

  • Use of systemic corticosteroids for other indications than COVID-19 in doses higher than 6 mg dexamethasone equivalents
  • Use of systemic corticosteroids for COVID-19 for 5 days consecutive days or more
  • Invasive fungal infection
  • Active tuberculosis
  • Fertile woman (<60 years of age) with positive urine human gonadotropin (hCG) or plasma-hCG
  • Known hypersensitivity to dexamethasone
  • Previously randomised into the COVID STEROID 2 trial
  • Informed consent not obtainable
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Dexamethasone 12 mgDexamethasoneIntravenous bolus injection of dexamethasone 12 mg once daily in addition to standard care for up to 10 days. We will allow the use of betamethasone 12 mg at sites, where dexamethasone is not available.
Dexamethasone 6 mgDexamethasoneIntravenous bolus injection of dexamethasone 6 mg once daily in addition to standard care for up to 10 days. We will allow the use of betamethasone 6 mg at sites, where dexamethasone is not available.
Primary Outcome Measures
NameTimeMethod
Days alive without life support at day 28Day 28 after randomisation

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

Secondary Outcome Measures
NameTimeMethod
All-cause mortality at day 28Day 28 after randomisation

Death from all causes

Days alive without life support at day 90Day 90 after randomisation

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

Number of participants with one or more serious adverse reactionsDay 28 after randomisation

Serious adverse reactions defined as new episodes of septic shock, invasive fungal infection, clinically important gastrointestinal bleeding or anaphylactic reaction

Days alive and out of hospital at day 90Day 90 after randomisation

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

Health-related quality of life at day 180Day 180 after randomisation

Assessed by EQ-VAS

All-cause mortality at day 90Day 90 after randomisation

Death from all causes

All-cause mortality at day 180Day 180 after randomisation

Death from all causes

Trial Locations

Locations (53)

Max Super Specialty Hospital, Saket

🇮🇳

New Delhi, India

Dept. of Anaesthesia and Intensive Care, Karolinska Universitetssjukhuset, Huddinge

🇸🇪

Stockholm, Sweden

Dept. of Infectious Diseases, Sahlgranska Universitetssjukhuset

🇸🇪

Göteborg, Sweden

Dept. of Infectious Diseases, Skånes Universitetssjukhus (SUS) Malmö

🇸🇪

Malmö, Sweden

Dept. of Anaesthesia and Intensive Care, Universitetssjukhuset i Linköping

🇸🇪

Linköping, Sweden

Dept. of Anaesthesia and Intensive Care, Danderyds Sjukhuset

🇸🇪

Stockholm, Sweden

Dept. of Cardiology, Södersjukhuset

🇸🇪

Stockholm, Sweden

Dept. of Infectious Diseases, Södersjukhuset

🇸🇪

Stockholm, Sweden

Dept. of Internal Medicine, Danderyds Sjukhuset

🇸🇪

Stockholm, Sweden

Apollo Hospital

🇮🇳

Chennai, India

Dept. of Anaesthesia and Intensive Care, Vrinnevisjukhuset, Norrköping

🇸🇪

Norrköping, Sweden

Dept. of Internal Medicine, Södersjukhuset

🇸🇪

Stockholm, Sweden

Dept. of Anaesthesia and Intensive Care, Skånes Universitetssjukhus (SUS) Malmö

🇸🇪

Malmö, Sweden

Dept. of Intensive Care Medicine, Bern University Hospital (Inselspital)

🇨🇭

Bern, Switzerland

Dept. of Anaesthesia and Intensive Care, Karolinska Universitetssjukhuset, Solna

🇸🇪

Stockholm, Sweden

Dept. of Infectious Diseases, Danderyds Sjukhuset

🇸🇪

Stockholm, Sweden

Dept. of Intensive Care, Nordsjællands Hospital - Hillerød, Denmark.

🇩🇰

Hillerød, Denmark

Dept. of Anaesthesia and Intensive Care, Lillebaelt Hospital

🇩🇰

Kolding, Denmark

Dept. of Intensive Care, Køge University Hospital

🇩🇰

Køge, Denmark

Dept of Intensive Care, Odense University Hospital

🇩🇰

Odense, Denmark

Dept. of Anaesthesia and Intensive Care, Zealand University Hospital Roskilde

🇩🇰

Roskilde, Denmark

Hvidovre Hospital - Dept of Intensive Care

🇩🇰

Hvidovre, Denmark

Hvidovre Hospital - Dept of Pulmonary Medicine

🇩🇰

Hvidovre, Denmark

Dept. of Anaesthesia and Intensive Care, Aalborg University Hospital, Denmark.

🇩🇰

Aalborg, Denmark

Dept. of Intensive care, Aarhus University Hospital

🇩🇰

Aarhus, Denmark

Dept. of Intensive Care, Copenhagen University Hospital, Rigshospitalet

🇩🇰

Copenhagen, Denmark

Dept. of Neuroanaesthesiology

🇩🇰

Copenhagen, Denmark

Dept. of Thoracic Anaesthesiology, Copenhagen University Hospital, Rigshospitalet

🇩🇰

Copenhagen, Denmark

Dept of Infectious diseases, Copenhagen University Hospital, Rigshospitalet

🇩🇰

Copenhagen, Denmark

Dept. of Intensive Care, Gentofte Hospital

🇩🇰

Hellerup, Denmark

Dept. of Anaesthesia and Intensive Care, Herlev Hospital

🇩🇰

Herlev, Denmark

Dept. of Anaesthesia, Regional Hospital West Jutland, Herning

🇩🇰

Herning, Denmark

Hvidovre Hospital - Dept of Infectious diseases

🇩🇰

Hvidovre, Denmark

Dept. of Anaesthesia, Slagelse Hospital

🇩🇰

Slagelse, Denmark

Dept. of Anaesthesia and Intensive Care, Viborg Hospital

🇩🇰

Viborg, Denmark

Jawahar Lal Nehru Medical Collega, AMU

🇮🇳

Aligarh, India

Amrita Institute of Medical Sciences

🇮🇳

Kochi, India

Bombay Hospital & Medical Research Centre

🇮🇳

Mumbai, India

Dept. of Anaesthesia and Intensive Care, Capio St Görans Sjukhus

🇸🇪

Stockholm, Sweden

Södersjukhuset

🇸🇪

Stockholm, Sweden

Dept. of Infectious Diseases, Karolinska Universitetssjukhuset, Solna

🇸🇪

Stockholm, Sweden

K. J. Somaiya Super Specialty Hospital

🇮🇳

Mumbai, India

P. D. Hinduja National Hospital & Medical Research Centre

🇮🇳

Mumbai, India

S L Raheja Fortis Hospital

🇮🇳

Mumbai, India

Tata Memorial Hospital

🇮🇳

Mumbai, India

Wockhardt hospitals

🇮🇳

Mumbai, India

Indraprastha Apollo Hospital

🇮🇳

New Delhi, India

Symbiosis University Hospital and Research Centre

🇮🇳

Pune, India

Rajendra Institute of Medical Sciences

🇮🇳

Ranchi, India

Gotri General Hospital

🇮🇳

Vadodara, India

Vishwaraj Hospital

🇮🇳

Pune, India

Christian Medical College Vellore

🇮🇳

Vellore, India

Dept. of Anaesthesia and Intensive Care, Sahlgranska Universitetssjukhuset

🇸🇪

Göteborg, Sweden

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