IRCT20080901001165N52招募中3 期
Investigating the efficacy of high dose of glucocorticoid in patients with moderate to severe pneumonia related to COVID-19
Bagheiat-allah University of Medical Sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 85 years(—)
- 性别
- All
入选标准
- •Confirmed diagnosis of COVID-19, with either lung CT-Scan result, which is typical for COVID-19 pulmonary involvement,or RT-PCR confirmation.
- •The patient has written consciously and freely consent to participate in the study;
- •The patient has moderate to severe Corona-Virus associated pneumonia;
- •In the first 48 hours of hospitalization, the patient did not show an improving trend;
- •In the first 48 hours after his/her inclusion into this study, there is no possibility of discharge from the patient's hospital;
排除标准
- •History of hypersensitivity reaction to glucocorticoids;
- •Recent hospitalization and treatment history due to COVID-19;
- •Receive antiviral drugs before including into this study, such as: Hydroxychloroquine, Kaletra, Ribavirin, Oseltamivir;
- •Receiving Methylprednisolone pulse before including into this study;
- •Uncontrolled severe chronic illnesses, including heart failure, kidney failure, liver failure, active cancer (history of chemotherapy within recent month), diabetes;
- •Receiving immunosuppressing /immunomodulating agents, such as systemic glucocorticoids.
研究者
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