CTRI/2022/11/047240尚未招募2 期
Pharmaceutical and Efficacy study of Ashtadashanga churna in Pulmonary fibrosisrelated with post covid and Post tuberculosis.
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
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.Patients able to take medicines orally.
- •2.Patients willing to provide informed consent shall be included.
- •3.Subjects of Post covid-19 will considered upto12 months from the date of RTPCR negative.
排除标准
- •1.Lung fibrosis caused by any other means such as lung cancer, lymphangitis carcinomatosis, bronchiectasis, COPD (chronic obstructive pulmonary diseases),connective tissue disorder, rheumatoid arthritis.
- •2.Pulmonary oedema
- •3.Subjects with severe vomiting which would make oral administration of medicine difficult.
- •4.Pregnant and lactating subjects.
- •5.Subjects with severe disease conditions like malignancy and those with advance liver or kidney diseases.
- •6.Initially included subjects who during the treatment develops severe other infective diseases or trauma etc.
- •7.Active cases of TB and COVID.
研究者
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