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临床试验/CTRI/2021/01/030639
CTRI/2021/01/030639已完成2 期

Validation of Standard Manufacturing procedure of Kamsaharitaki avaleha prepared by two different varieties of Haritaki and their comparative effect on Tamaka Shwasa, A Double Blind Randomized Clinical Trial.

Director0 个研究点目标入组 61 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
61

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 presenting with minimum 3 to 4 classical signs and symptoms of Tamaka Shwasa.
  • 2. Mild persistent cases of asthma (as per WHO GINA guidelines) of duration more than 6 months.

排除标准

  • 1.Age more than 60 years and below 18years.
  • 2.Mild intermittent, moderated persistent, severe persistent to severe asthma.
  • 3.Dyspnoea resulting from other diseases like left ventricular failure, COPD (chronic bronchitis, emphysema), upper respiratory tract obstruction, bronchiectasis, etc.
  • 4.Patients on regular steroidal therapy, inhalers or bronchodilators.
  • 5.Patients having pneumonia, tuberculosis, lung cancer, lung abscess and another such complicated conditions.
  • 6.Patients having diabetes, hypertension, acute and chronic renal failure etc. conditions in which urination is markedly diminished or excessive were excluded.
  • 7.HIV positive patients.
  • 8.Pregnant/lactating mothers

研究者

发起方
Director

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