IRCT20211203053263N1已完成3 期
Comparison of Bosentan with routine protocol on outcomes of high-risk outpatients with COVID-19 infection.
Ilam University of Medical Sciences0 个研究点目标入组 350 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 350
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
- •One or more symptoms of COVID-19 illness and laboratory-confirmed SARS-CoV-2 determined by PCR assay < 72 hours prior to randomization
- •Has at least one CDC defined risk factor for severe COVID-19 illness
- •Clinical team deems stable for outpatient management without supplemental oxygen
- •Has informed consent
- •women of child bearing potential must agree to use at least one primary form of contraception for the duration of the study
排除标准
- •Pregnancy or Lactation
- •Glibenclamide Consumption
- •Cyclosporine Consumption
- •Aminotransferases > 3 times normal
- •Allergy to bosentan
研究者
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