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临床试验/IRCT20211203053263N1
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

发起方
Ilam University of Medical Sciences

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Bosentan for high-risk outpatients with COVID-19 | 临床试验