跳至主要内容
临床试验/ACTRN12621001200875
ACTRN12621001200875招募中2 期

A randomised controlled trial of Dexamethasone for Emergency and Life-Threatening Admissions due to COVID-19 in Virtual Care: the DELTA study

Royal Prince Alfred Hospital0 个研究点目标入组 650 人开始时间: 2021年9月8日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
650

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Adult patients (age greater than or equal to 18 years)
  • -Currently under the care of RPAV in the community or 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, chest pain, lethargy, dizziness, myalgia, anosmia, dyspnea, headache, gastrointestinal symptoms), with no requirement for oxygen or hospitalization
  • -Requiring nursing or medical assessment by RPA Virtual Hospital clinicians within 72 hours for new or escalating symptoms of mild to moderate COVID-19

排除标准

  • -Currently taking oral or inhaled corticosteroids
  • -Major medical or psychiatric comorbidities 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 for 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

研究者

相似试验