跳至主要内容
临床试验/CTRI/2020/08/027162
CTRI/2020/08/027162已完成2 期

An Open-Label, Prospective, Randomized, Comparative, Parallel Group, Multi-Center, Proof of Concept Study to Assess the Efficacy and Safety of Inosine Pranobex Added to Current Standard of Care (CSC) in COVID-19 Patients.

Themis Medicare0 个研究点目标入组 83 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
83

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

入选标准

  • 1.Written signed and dated informed consent (patient or LAR).
  • 2.Either gender, in the age group between 18 to 65 years
  • 3.Patients of laboratory confirmed COVID-19 [nasopharyngeal (preferred) or oropharyngeal swab RT-PCR positive] presenting with WHO listed symptoms of COVID-19 c/o fever, headache, myalgia, cough, throat pain or shortness of breath
  • 4.A score of between 3 to 5 on the WHO Modified Ordinal Scale for Clinical Improvement (refer protocol appendix 23.1)
  • 5.SpO2 >=90% for adults and respiratory rate <= 30/minute
  • 6.Patients who provide a agree to abide by the study requirements

排除标准

  • 1.Known hypersensitivity to any of the ingredients of the study drug
  • 2.Pregnant and lactating women
  • 3.Children <18 yrs. of age; elderly >65 years
  • 4.SpO2 <90% for adults and respiratory rate >30/minute
  • 5.History of gout or hyperuricemia (serum uric acid level >6mg/dl), urolithiasis, nephrolithiasis or any degree of renal dysfunction
  • 6.Patients with history of diagnosed primary congenital immunodeficiency, or acquired immunodeficiency like HIV, OR any Genetic or developmental anomaly like Cerebral Palsy, coeliac disease, lactose intolerant, cancer in nor remission stage.
  • 7.Patient who are undergoing treatment with xanthine oxidase inhibitors, uricosuric agents, diuretics, immunosuppressive agents or zidovudine.
  • 8.Patients with severe cardiac, hepatic, gastrointestinal, renal, pulmonary and skin diseases.
  • 9.Patients simultaneously participating in another clinical study.
  • 10.Medical or psychological conditions deemed by the investigators to interfere with successful participation in the study
  • 11.A subject who is judged by the investigator as inappropriate to participate in the study for any reason other than those mentioned above

研究者

发起方
Themis Medicare

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