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. 2022 Nov 17;2022(11):CD014963. doi: 10.1002/14651858.CD014963.pub2

ACTRN12621001200875.

Study name A randomised controlled trial of dexamethasone for emergency and life‐threatening admissions due to COVID‐19 in virtual care: the DELTA study
Methods Trial design: triple‐blind, randomised controlled trial
Sample size: 650
Setting: outpatient
Language: English
Number of centres: not stated
Type of intervention (treatment/prevention): treatment
Participants Inclusion criteria:
  • Adult patients (age greater than or equal to 18 years)

  • Currently in Special Health Accommodation (SHA)

  • Confirmed COVID‐19 on polymerase chain reaction (PCR) testing within the last 14 days

  • Exhibiting mild/moderate COVID‐19 symptoms (fever, respiratory tract symptoms, dyspnoea, headache, gastrointestinal symptoms), with no requirement for oxygen or hospitalisation

  • Within 72 hours of onset of mild/moderate COVID‐19 symptoms

  • Requiring medical consultation by RPA Virtual Hospital doctors


Exclusion criteria:
  • Currently taking oral or inhaled corticosteroids

  • Major medical or psychiatric co‐morbidities precluding the use of corticosteroids (e.g. poorly controlled diabetes mellitus, chronic heart disease, chronic renal disease, chronic liver failure, schizophrenia or thought disorder, bipolar disorder)

  • Immunosuppression or treatment for malignancy

  • Hypersensitivity to corticosteroids, thiamine, wheat, lactose, povidone, maize starch or magnesium stearate

  • History of alcohol dependence or at risk alcohol intake

  • At risk of thiamine deficiency (e.g. eating disorders, chronic malabsorption)

  • Requires urgent transfer to the emergency department at the time of assessment

  • Patient declines or is unable to provide consent

  • Lactating or pregnant women

  • No access to a personal or loaned electronic device

  • Unable to read or write English

Interventions Details of intervention: dexamethasone plus usual care
  • Dose: 6 mg per day, for 2 days

  • Route of administration: oral


Treatment details of control group (e.g. dose, route of administration): probably placebo (not explicitly explained)
Concomitant therapy: not stated
Outcomes Primary study outcome: COVID‐19 related hospitalisation, defined as COVID‐19 related emergency presentation (excluding injuries and presentations for social reasons), or hospital admission or intensive care unit admission or death
Starting date 20 September 2021
Contact information Prof Michael Dinh
Royal Prince Alfred Hospital Level 10, King George V Building, Camperdown, New South Wales 2050 Australia
Telephone: +61 419620654
Email: Michael.Dinh@health.nsw.gov.au
Notes Recruitment status: recruiting
Prospective completion date: not stated
Date last update was posted: 10 December 2021
Sponsor/funding: Royal Prince Alfred Hospital