RPCEC00000334已完成未知
Safety and effectiveness of BIOMODULIN T in protective therapy in events of local transmission of COVID-19. Interventional Study (COVID-19)
Centro Nacional de Biopreparados (BioCen)0 个研究点开始时间: 2020年9月10日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
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
- Non-randomized controlled trial. Masking: Open. Control group: Uncontrolled. Assignment: Parallel. Purpose: Prevention
入排标准
- 年龄范围
- 60 years 至 one（—）
- 性别
- All
入选标准
- •1. Age 60 years and over.
- •2. Any sex and skin color.
- •3. Patients who express their consent in writing, to participate in the study and in the event that major cognitive impairment is present, be signed by a family member, tutor or caregiver.
排除标准
- •1. Patients who have received treatment with BIOMODULINA T® in the previous two months.
- •2. Patients with known hypersensitivity to any component of the formulation.
- •3. Patients with acute allergic states or history of severe allergic reactions.
- •4. Patients with uncontrolled intercurrent illnesses including, but not limited to: acute infections with concomitant febrile symptoms, symptomatic congestive heart failure, unstable angina pectoris.
研究者
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