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Clinical Trial of Efficacy of Dashmoola Haritaki Avaleha in Tamaka Shwasa with special reference to Bronchial Asthma

Phase 3
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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
•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
NameTimeMethod
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.
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