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A clinical study on the effect of Shirisha Bharangyadi Kashaya alone and along with Vasadi Arka nebulization in asthma

Standardization and A comparitive clinical study of Shirisha Bharangyadi Kashaya with and without Vasadi Arka nebulization in tamaka Shwasa (Bronchial Asthma) - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100862
Enrollment
64
Registered
2026-01-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: J454- Moderate persistent asthma

Interventions

None listed

Sponsors

Department of Dravyaguna Faculty of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient with stable bronchial asthma asper WHO GINA Guidelines for atleast 6 weeks prior to study entry positive test of reversibility FEV1 more than 50 and less than 80 FEV1 and FEV ratio less than 70

Exclusion criteria

Exclusion criteria: Patients with PEFR less than 50 or FEV lessthan 50 patient having pulmonary diseases other than asthma like COPD,fibrotic lung disease,lung TB etc. Pregnant and lactating women Patient with poorly controlled diabetes Patient with poorly controlled HTN(systolic greater than 160 and diastolic greater than 100 Patients on prolonged medications (greater than 6 weeks) that may have influence on the outcome of the study Smoker or alcoholic or drug abuser Patients who have past history of Atrial fibrillation,acute coronary syndrome,MI,stroke or severe arrythmia in last 6 months Patient having systemic illness necessiating long term drug treatment like TB,carcinoma,endocrine disorders etc. Patients who have completed participation in any otherclinical trial during past 6 months. Patient having SPO2 less than 90 Emergency patients requiring O2 nebulization

Design outcomes

Primary

MeasureTime frame
The primary outcome measure include improvement in asthma symptoms and pulmonary function measured by Grading Analog Scale (GAS), Asthma control test(ACT) and PFTsTimepoint: 90 days study with follow up every 1 month

Secondary

MeasureTime frame
Health-related QOL will be our secondary outcome measure.Timepoint: 90 days study with follow up every 1 month

Countries

India

Contacts

Public ContactDr Poonam Sharma

Banaras Hindu university

bhavanashetty2308@gmail.com8618931237

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026