跳至主要内容
临床试验/CTRI/2020/01/022659
CTRI/2020/01/022659已完成2 期

An open label clinical trial to evaluate the Efficacy of Kuka Cough Syrup in the Patients Suffering with Kasa (Acute Cough and Throat Irritation)

Multani Pharmaceuticals Ltd0 个研究点目标入组 46 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
46

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

  • History of acute nonproductive cough due to any cause.
  • Subjects who are willing to give informed consent and ready to comply with the protocol.
  • Subjects who are ready to provide regular follow up until the completion of the study.

排除标准

  • Participants with a history of acute lower respiratory tract infections such as pneumonia, bronchitis whooping cough, chronic obstructive pulmonary disease/asthma, tuberculosis, systemic bacterial infections for which specific drug therapy required Any underlying lung pathology such as lung abscess or cystic fibrosis, individuals with a history of myocardial infarction within 4 weeks prior to enrollment;

研究者

发起方
Multani Pharmaceuticals Ltd

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