Clinical Trial of Efficacy of Dashmoola Haritaki Avaleha in Tamaka Shwasa with special reference to Bronchial Asthma
- Conditions
- Health Condition 1: J454- Moderate persistent asthma
- Registration Number
- CTRI/2024/04/065734
- Lead Sponsor
- Dr Salma Momin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Patients with Classical signs and symptoms of Tamaka Shwasa with special reference to bronchial asthma
2.Age group 20-70yrs
3.Either Gender
4.Mild and moderate grade of Bronchial Asthma as per GINA
5.Patient indicated for Koshta Shodhana
6.Patient willing to participate with Written Consent.
1.The patients diagnosed with COPD ( Chronic bronchitis, Emphysema), Pneumonia, Cardiac asthma, Tuberculosis, Pleural effusion, Cardiac pathology.
2.Patients with Status Asthamaticus
3.Patients with Diabetes Mellitus and Hypertension, Uraemia, Acidosis, Malignancy .
4.Pregnant Woman, Lactating Woman
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method •To evaluate the efficacy of Dashmoola Haritaki Avaleha in Tamaka Shwasa with special reference to Bronchial Asthma. <br/ ><br>•To compare the effect of Dashmoola Haritaki Avaleha and Vasa Avaleha in Tamaka Shwasa with special reference to Bronchial Asthma. <br/ ><br>•To compare the effect of Dashmoola Haritaki Avaleha and Vasa Avaleha in Health related Quality of Life According to GINA Guidelines. <br/ ><br>Timepoint: Subjective parameters will be assessed on <br/ ><br>baseline on 0th day ,2nd week and 4th week and 45th day of <br/ ><br>the intervention. <br/ ><br>
- Secondary Outcome Measures
Name Time Method CBC ESR AEC and SPIROMETERY test will be done on 0th day and 45th day of the intervention.Timepoint: Objective parameters will be assessed on <br/ ><br>baseline on 0th day ,2nd week and 4th week and 45th day of <br/ ><br>the intervention.