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A Clinical study to evaluate the efficacy of Amrutadi vati and Vasadi vati in the treatment of Bronchial Asthma(Shwasa).

A clinical study of Amrutadi vati and Vasadi vati in the management of Tamaka shwasa w.s.r. to Bronchial asthma

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/08/004927
Enrollment
60
Registered
2014-08-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Bronchial Asthma

Interventions

Intervention1: Amrutadi vati: orally 2tab.(500mg each) tds after food with luke warm water for 8weeks follow up 4weeks Control Intervention1: Vasadi vati: orally 2tab.(500mg each) tds after food with

Sponsors

POST GRADUATE TEACHING HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex aged between 16 to 70 years Patients having signs and symptoms of Tamak shwasa described in ayurvedic texts and modern texts will be included.

Exclusion criteria

Exclusion criteria: Patients of age less than 16 and above 70 years Patients with status asthmaticus asthma due to cardiac origin Patients having complications like cor pulmonale emphysema pneumonia tuberculosis and malignancy etc and breathlessness due to diabetes mellitus severe anaemia renal failure major endocrine disorders will be excluded from the study

Design outcomes

Primary

MeasureTime frame
Change in the clinical symptoms of Bronchial Asthma like Dyspnoea Wheezing Coughing Chest tightness etcTimepoint: 8 weeks study and 4 weeks follow up

Secondary

MeasureTime frame
Change in SpirometryTimepoint: 8 weeks study and 4 weeks follow up

Countries

India

Contacts

Public ContactDr Alankruta R Dave

Institute for Post Graduate Teaching and Research in Ayurveda

alankruta@yahoo.com9824171817

Outcome results

None listed

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