跳至主要内容
临床试验/CTRI/2018/04/012980
CTRI/2018/04/012980已完成2 期

A Clinical Evaluation of Efficacy and Safety of AyuAsmo Capsules in Patients Suffering From Bronchial Asthma.

Welex Laboratories Pvt Ltd0 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
2 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

  • 2.Patients with diagnosis of bronchial asthma, for a period of at least 6 months prior to screening visit.
  • 3.Patients not on continue use of inhalers bronchodilators.
  • 4.Percentage FEV1 more than 50% of prediction (predicted values) on screening visit.
  • 5.Subjects willing to give informed consent and ready to comply with the study protocol.

排除标准

  • 1.Known cases of severe/chronic diseases those interfere with study.
  • 2.Known cases of active malignancy.
  • 3.Subjects giving history of significant cardiovascular event less than 12 weeks prior to screening.
  • 4.Known cases of chronic cardiac illnesses
  • 5.Subjects having known chronic, contagious infectious disease, such as active tuberculosis, Hepatitis B or C, or HIV.
  • 6.Subjects with uncontrolled diabetes and hypertension.
  • 7.Subjects using any other investigational drug within 1 month prior to recruitment in this study.
  • 8.Known hypersensitivity to any of the ingredients used in study drug.
  • 9.Pregnant and Lactating females.
  • 10.Subjects currently participating in any other clinical study.
  • 11.Any other condition due to which patients are deemed to be unsuitable by the investigator for reason(s) not specifically stated in the exclusion criteria.

研究者

发起方
Welex Laboratories Pvt Ltd

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