IRCT20080901001165N64尚未招募3 期
Evaluation of efficacy and safety of Glurunic acid (G2013) in patients with COVID-19
Ministry of Defense, Department of Health0 个研究点目标入组 180 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 180
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 65 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/Legal guardian has written consciously and freely consent to participate in the study;
- •In the first 48 hours after his/her inclusion into this study, there is no possibility of discharge from the patient's hospital;
- •Moderate to severe COVID pneumonia
排除标准
- •The patient is present at another clinical trial at the same time.
- •Severe renal impairment
- •Severe hepatic impairment
- •Severe cardiac impairment
- •Uncontrolled diabetes
- •Active infection
- •Active cancer
- •Coagulopathy
- •Primary immunodeficiency syndrome
- •Allergy to Glurunic acid
研究者
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