Effect of Ayurveda treatment in the Management of Tamaka Shwasa(Bronchial Asthma)
- Conditions
- Health Condition 1: J454- Moderate persistent asthma
- Registration Number
- CTRI/2022/07/044267
- Lead Sponsor
- ational Institute of Ayurveda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
•Patients willing to participate and sign consent in the clinical trial.
•Patients in the age group of 18-65 yrs.
•Patients with Intermittent, mild-persistent & moderate-persistent asthma and are not on regular medication for Asthma.
•Patients having FEV1 > 60% of predicted value
•Patients of Rhinitis with spirometric evidence of reversible airflow obstruction.
•Patients who have not received any AYUSH intervention in last 15 days for related symptoms
•Patients having severe persistent (FEV1 <60 % of predicted) and Acute exacerbation of asthma
•Diagnosed cases of tuberculosis, pneumonia, COPD and other acute and chronic pulmonary disorders
•K/c/o malignancies of the respiratory and other system.
•Patients who have consumed AYUSH intervention for related complaints in last 15 days.
•Patients on regular anti allergic medications, on regular inhaled, intranasal or oral steroids.
•Patients on immunotherapy for allergy.
•Patients with Haemoglobin less than 9 mg/dl.
•Patients having concomitant systemic illness like uncontrolled Hypertension, Poorly controlled Diabetes Mellitus, Renal failure, Malignancy, Acute or Chronic liver disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method â?¢Forced Expiratory Volume in first second (FEV1) from baseline values.Timepoint: 56 days
- Secondary Outcome Measures
Name Time Method â?¢Improvement in Peak expiratory flow rate (PEFR). <br/ ><br>â?¢Changes in IgE & Absolute Eosinophil count <br/ ><br>â?¢Degree of improvement in asthma related symptoms on the basis of Asthma control questionnaire (ACQ) <br/ ><br>â?¢Degree of Improvement in Total Nasal Symptom Score (TNSS) <br/ ><br>Timepoint: 56 days