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Role of Ayurvedic drug â??AYUSH-Aâ?? in the Management of Bronchial Asthma (TamakaShwasa)

Phase 2
Conditions
Health Condition 1: J452- Mild intermittent asthma
Registration Number
CTRI/2021/06/034446
Lead Sponsor
CENTRAL COUNCIL FOR RESEARCH IN AYURVEDIC SCIENCES MINISTRY OF AYUSH GOVERNMENT OF INDIA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patients of any gender with age between 18 to 60 years.

2.Patients with mild tomoderate stable Bronchial Asthma (TamakaSwasa) (as per GINA

Guidelines 2020 recommendations) and on regular and stable dose of inhaled therapy (medium â?? high dose ICS alone or ICS+LABA) for at least 4 weeks prior to study entry.

3.Patients willing to participate and provide written consent.

Exclusion Criteria

1.Patients with H/O acute exacerbation of respiratory symptoms during last four weeks

2.Patients with evidence of malignancy.

3.Chronic obstructive pulmonary disease, pneumonia, lung cancer and other chronic lung diseases

4.Patients under treatment for Pulmonary TB or with a diagnosis of Pulmonary TB.

5.Patients with uncontrolled Diabetes Mellitus assessed by fasting blood sugar or HbA1c >7.5%.

6.Patients with unstable cardiovascular disease.

7.Patients suffering from other major systemic illness necessitating long term drug treatment (eg: Rheumatoid arthritis, Psycho-Neuro-Endocrinal disorders, etc.)

8.Pulmonary emphysema, chronic obstructive pulmonary disease, pulmonary emphysema, pulmonary heart disease, pneumonia, lung cancer and other lung diseases

9.Patients with concurrent serious hepatic disorder or Renal Disorders

10.Active smokers, alcoholics and/or any form of drug abusers

11.H/o hypersensitivity to the trial drug or any of its ingredients.

12.Pregnancy or lactating women.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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