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临床试验/IRCT20080901001165N52
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

发起方
Bagheiat-allah University of Medical Sciences

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