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Use of Vasa swaras bhavit vardhaman Pippali in patients of Tamak Shwas

A clinical study of Tamak Shwas W.S.R to Bronchial Asthma, with trail drug Vasa Swaras Bhavit Vardhman Pippali a single group clinical trial - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086850
Enrollment
30
Registered
2025-05-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: J453- Mild persistent asthma

Interventions

None listed

Sponsors

Government Akhandanand Ayurved College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Both male & female Patients having age greater than or equal to 18years and less than or equal to 60 years of age Patient with chronicity of Tamaka Shwasa Less than 5 years. Patients with classical signs and symptoms of Tamaka Shwasa described in ancient Ayurveda text will be selected for present study such as ShwasaKrichchhata (Dyspnoea) Ghurghurukama (Wheezing sound) Kasa (Cough) Asamyakanidra (Disturbedsleep) Kantodhwamsa (Hoarseness of voice) Pinasa (Coryza) ShleshmaVimokshanteMuhurtam Sukham (After expectoration patient feels better). ParshvaAvgrihyate (Chest tightness) Aasinolabhatesaukhyama (Comfortable in sitting position) Meghambusheetpragvataihi abhivardhate(increase symptoms after weather change) 4.PEF greater than or equal to 50 %

Exclusion criteria

Exclusion criteria: Acute Dyspnoea, Relative Hypoxia And Cyanosis (Status Asthmaticus). Patients suffering from any systemic or chronic illness like Emphysema, Type 2diabetes mellitus, Hypertension, Renal diseases and Cardiac diseases. Patients of Cor pulmonale, Pulmonary Hypertension, Cardiac Asthma and with severe exacerbation. Any acute systemic disease or Infection, post long covid lung disease/complication. Pregnant and lactating mothers. Any malignancy. Acute & serious conditions require immediate intervention will be excluded. PEF less than 50% ILD (Interstitial Lung Disease) Pulmonary Fibrosis and Consolidation Chronicity More Than 5 Year

Design outcomes

Primary

MeasureTime frame
Results will be assessed on the basis of gradation of clinical features of Tamaka ShwasaTimepoint: 7 days 14 days 21 days 30 days 40 days

Secondary

MeasureTime frame
Peak flow meter reading to access improvement of lung functionsTimepoint: 2 weeks of completion of clinical trial or treatment

Countries

India

Contacts

Public ContactDr Surendra A Soni

Government Akhandanand Ayurved College and Hospital

surendraasoni@gmail.com9408441150

Outcome results

None listed

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