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
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
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