None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: apprantly healthy person
Exclusion criteria
Exclusion criteria: i. Volunteers having acute respiratory disease and chronic respiratory disease. ii. Any other additional disease (Hypertension, Diabetes Mellitus, Asthma, Chronic Renal Failure, Peptic Ulcer, Hernia, Lung Abscess, Tuberculosis, Malignancy, etc.) iii. Pregnant& Lactating Mother iv. Volunteers who are currently participating or have completed participation in any other clinical trial during the past six months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| after the 30 days of trial group A will have more increase in lung capacity than Group BTimepoint: at baseline, the end of study & after the 15 days of follow up | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Improvement in quality of life in both the groupTimepoint: at the end of study | — |
Countries
India
Contacts
all India Institute of Ayurveda