跳至主要内容
临床试验/CTRI/2020/07/026434
CTRI/2020/07/026434已完成3 期

A prospective, single arm, multicentric clinical study to evaluate the safety and efficacy ofHERBOVIR syrup in subjects with upper respiratory tract infection along with standard of care

VENKAT PHARMA0 个研究点目标入组 0 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

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.Subjects aged 18-65 years of age and of either sex
  • 2.subjects who were disposed to give consent to the study and willing for follow-up
  • 3.Subjects who are willing to sign ICF
  • 4.Clinical signs and symptoms of an URTI with a duration of up to 24 hours accompanied with or without fever 37.5 C (axillary body temperature) or higher
  • 5.At least 1 of 3 types of URTI symptoms â?? Nasal (plugged nose, runny nose, sneezing), Pharyngeal (scratchy throat, sore throat, pharyngeal hyperaemia), Cough (ordinary cough without suspicion of acute lower respiratory tract disease). At least 1 of 5 general symptoms â?? feeling tired, weakness, body ache, irritable or whiney,or less active
  • 6.Not be in need of hospitalized medical care at screening

排除标准

  • 1.Age less than 18 years and more than 65 years
  • 2.Pregnancy
  • 3.Severe or complicated course of URTI.
  • 4.Signs of acute lower respiratory tract disease.
  • 5.Daily use of antibiotics, steroids and cytotoxic agents.
  • 6.Any uncontrolled systemic disease, infection
  • 7.Those with serious Cardiovascular, Cerebrovascular, Respiratory, Liver or Renal disease• or any other disorder

研究者

发起方
VENKAT PHARMA

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