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临床试验/IRCT20200328046886N3
IRCT20200328046886N3招募中3 期

Evaluation of the Efficacy and safety of dolutegravir in patients with moderate COVID-19 disease (randomized double blind placebo controlled trial)

Mazandaran University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
100

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 80 years(—)
性别
All

入选标准

  • 1) Aged between 18 to 80
  • 2) Patients with definitive diagnosis of covid-19 (Lung involvement in Covid-19 compliant CT confirmed by coronavirus pneumonia).
  • 3) =8 days since illness onset
  • 4) Having one of the following symptoms: Fever (= 37.8 ° C at any time), Dry cough, Shortness of breath, Fatigue
  • 5) One of the following: Involvement of 3 or more lobes of the pulmonary lobes, >O2Sat< 94%
  • 6) Patients with signing Informed Consent Form Willing

排除标准

  • 1) Severe hepatic impairment (Child-pough C)
  • 2) Patients taking Phenytoin, Fosphenytoin, Oxcarbazepine, Phenobarbital, Primidone and St John's Wort
  • 3) History of disease because of COVID-19
  • 4) History of taking Covid-19 experimental drug
  • 5) lactation
  • 6) Requires intubation at admission
  • 7) Sensitivity to Dolutegravir
  • 8) Severe disability that prevents cooperation
  • 9) Patient dissatisfaction with the study

研究者

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