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临床试验/IRCT20200818048444N1
IRCT20200818048444N1已完成3 期

Verification of the efficacy of Bromhexine-hydrochloride in treatment of patients with COVID19 disease

Tabriz University of Medical Sciences0 个研究点目标入组 1,300 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
1,300

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

  • 18 years and older, both sexes
  • Having home contact, unmasked contact with a patient with Covid-19 confirmed by RT-PCR or clinical evidence or radiography of pneumonia and acute respiratory distress syndrome (ARDS);
  • No clinical signs of Covid-19 (fever, cough, dyspnea, shortness of breath, sore throat, extreme tiredness, digestive problems);
  • No chronic respiratory problems or other illnesses that are mistaken for symptoms of COVID-19

排除标准

  • Involvement with any other ongoing studies.
  • Pregnant or breast feeding woman or with positive pregnancy test result for fetal safety
  • Severe liver disease as a strong confounding factor
  • Severe renal failure as a strong confounding factor
  • Refusal by attending physician for no clinical equipoise
  • Advanced active malignancy as a strong confounding factor
  • Patient in other clinical trials for COVID-19 within 30 days before/after ICF as a confounding factor/s
  • Other patient characteristics (not thought to be related to underlying COVID-19) that portend a very poor prognosis (e.g, severe liver failure, severe renal failure, and etc. May impact primary and other clinical endpoints- Known allergy to study drug or its ingredients related to renin-angiotensin system (RAS), or frequent and/or severe allergic reactions with multiple medications for patient protection purposes
  • Other uncontrolled disease, as judged by investigators that may influence study endpoint and other clinical outcome

研究者

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