IRCT20201004048922N1招募中3 期
Evaluation of the effectiveness of intravenous infusion of human COVID-19 hyperimmune plasma with specific antibody titer in hospitalized patients with Covid-19: a randomized clinical trial
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 75
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 no limit（—）
- 性别
- All
入选标准
- •Confirmed or suspected COVID-19 pneumonia based on PCR or pulmonary imaging;
- •Presenting clinical symptoms of COVID-19 (fever, cough, dyspnea);
- •O2 saturation equal or less than 93%;
- •Age equal or more than 18 years old;
- •The patient has informed and free written consent to participate in the study;
- •Less than 7 days passed from the onset of clinical symptoms to the time of enrollment;
- •The patient should not attend another clinical trial at the same time.
排除标准
- •Advanced renal or liver disease;
- •Active cancer;
- •Known Hypersensitivity reaction to Plasma-derived drugs;
- •The patient may be excluded from the study during the first 48 hours.
研究者
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