RPCEC00000330尚未招募2 期
Evaluation of the effect and safety of the CIGB-258 peptide in the treatment of seriously or critically ill patients due to COVID-19. (COVID-19)
Center for Genetic Engineering and Biotechnology (CIGB), in Havana0 个研究点目标入组 60 人开始时间: 2020年8月11日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled trial. Masking: Open. Control group: Active. Assignment: Parallel. Purpose: Treatment
入排标准
- 年龄范围
- 18 years 至 one（—）
- 性别
- All
入选标准
- •1) Patients aged = 18 years.
- •2) Virological diagnosis by RT-PCR of infection to SARS-CoV-2.
- •3) Patients in serious or critical condition.
- •4) Acute respiratory failure according to clinical and Berlin criteria (imaging and oxygenation).
- •5) Voluntariness of the patient through informed consent.
排除标准
- •1) Previous treatment with JAK inhibitor, tocilizumab or other anti-IL6R or IL-6, IL-1 inhibitor (Anakinra).
- •2) Patients with kidney disease on hemodialysis.
- •3) Patients who previously indicate NO intubation, NO resuscitation.
- •4) Known hypersensitivity to any of the components of the formulations under study.
- •5) Pregnancy or breastfeeding.
研究者
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