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
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