CTRI/2021/02/031541已完成未知
A study on the efficacy and adverse effects of Injection Remdesivir in moderate to severe SARS CoV-2 pneumonia in a tertiary care hospital in Kolkata.
nil0 个研究点目标入组 63 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 63
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •1.Age =18 years at time of signing Informed Consent Form
- •2.Laboratory (RT-PCR) confirmed COVID-19.
- •3.Lung involvement confirmed with chest imaging
- •4.Hospitalized with a SaO2/SPO2=94% on room air or Pa02/Fi02 ratio <300mgHg
- •5.=12 days since illness onset
- •6.Have given consent to participate in the study.
排除标准
- •1.Severe liver disease (e.g. Child Pugh score = C, AST >5 times upper limit)
- •2.Pregnant or breastfeeding, or positive pregnancy test in a pre dose examination
- •3.Patients with known severe renal impairment (estimated glomerular filtration rate =30 mL/min/1.73 m2) or receiving continuous renal replacement therapy, hemodialysis, peritoneal dialysis
- •4.Receipt of any experimental treatment for COVID-19 within the 30 days prior to the time of the screening evaluation.
研究者
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