Skip to content

Clinical trial to study the combined effect of Ayurvedic formulations in Bronchial Asthma.

An Open label, Single arm, Interventional trial to study the Efficacy and Safety of Shwasakuthara rasa and Kasahara kashaya in Tamaka Shwasa W.S.R. to Bronchial Asthma. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067896
Enrollment
30
Registered
2024-05-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J452- Mild intermittent asthma

Interventions

None listed

Sponsors

National Institute of Ayurveda Deemed to be University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of either sex in age group of 18-60 years. 2. patients with intermittent, mild- persistent and moderate persistent asthma according to GINA classification. 3.Patients presenting with symptoms of allergic rhinitis and having associated asthma symptoms as per GINA classification. 4.Patients who have not received any AYUSH intervention in last 15 days for related symptoms.

Exclusion criteria

Exclusion criteria: 1.Patients having acute exacerbation of asthma at the time of recruitment. 2.Patients having severe persistent asthma as per GINA classification. 3.Patient having any acute respiratory infection or have received any modern medication for such illness in last 15 days. 4.Patients having past or recent diagnosis/treatment of tuberculosis, pneumonia, COPD, bronchiectasis. 5.Patient having history of any hypersensitivity to any of the ingredient/s of the trial drugs. 6.Patients having history or diagnosis of any type of malignancy. 7.Patients on regular anti allergic medications. 8.Patients receiving aspirin, oral corticosteroids or are on regular inhaled corticosteroids. 9.Patients on immunotherapy for allergy. 10.Patients with Hemoglobin less than 9.0 g/dl. 11.Patients having concomitant systemic illness like uncontrolled hypertension, poorly controlled diabetes, renal failure, and severe acute or chronic liver disease. 12.Pregnant and lactating mothers

Design outcomes

Primary

MeasureTime frame
Changes in Asthma control questionnaire (ACQ) score from baseline value at the end of 4th week.Timepoint: 0,2 week,4 week

Secondary

MeasureTime frame
Changes in Peak expiratory flow rate (PEFR) and FEV1 and FVC; in Fractional exhaled Nitric Oxide (FeNO) value; in Absolute Eosinophil count, IgE value from baseline value at the end of 4th weeks. Changes in Asthma Quality of Life (AQLQ) score from baseline value at the end of 4th week. Average reduction in use of rescue medication from baseline score at the end of 4th week. Timepoint: 0,2 week,4 week

Countries

India

Contacts

Public ContactDr Deval Kevadiya

National Institute of Ayurveda, Deemed to be University, Jaipur

dr.abhishek82@gmail.com9915613039

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026