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Use of swashahara mahakashaya avleha in childhood bronchial asthma

A Comparative Study to Evaluate the Efficacy of Shwasahara Mahakashaya Avleha w.r.to Shwasahara Mahakashaya choorna in Tamaka Shwasa w.s.r to Childhood Bronchial Asthmaâ??An open ended, double armed, Randomized, Controlled Clinical Trial.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/06/019745
Enrollment
60
Registered
2019-06-18
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: J454- Moderate persistent asthma

Interventions

Intervention1: Shwasahara mahakashaya avleha: Age in years Drug doses in 3 doses 5-7 6gm 8-10 9gm 11-13 12gm 14-15 15gm ORAL

Sponsors

All India Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Individuals of either gender between age group of 5 to 15 years. 2) Diagnosed cases of Tamaka Shwasa â??bronchial asthma with at least 3 episodes of asthma symptoms (cough, breathlessness) during the previous year. 3) Severity as mild to moderate stable bronchial asthma (Tamaka Shwasa) as per W.H.O GINA Guidelines. 4) Patient on other drug therapy will be included only after completion of the washout period of 3 weeks. 5) Parents giving consent to participate in study.

Exclusion criteria

Exclusion criteria: 1. Individuals below 5 years and above 15 years of age. 2. Sever case like status asthmaticus. 3. Evidence of active concomitants pulmonary disease other than asthma. 4. Evidence of requirement of intubation for asthma, or had been hospitalized for asthma within 1 month before. Had unresolved sinus disease or an unresolved upper or lower respiratory tract infection within 3 weeks. 5. More than 4 short courses of oral corticosteroids within the year preceding the screening visit or any oral corticosteroids in the preceding 4 weeks. 6. Concomitant severe decompensated systemic disease (cardiovascular, renal, hepatic, endocrine, haematological, neurological, immunological). 7. Patient/Parents not willing to participate in the study.

Design outcomes

Secondary

MeasureTime frame
1-Asthma control questionaire 2-GINA asthma guidelines 3-Ayurvedic parameters like Dasavidha parikshya,Astasthana parikshya 4-pulmonary function test and peak expiratory flow examinationTimepoint: oday,60 day an one during follow up;1-Asthma control questionaire 2-GINA asthma guidelines 3-Ayurvedic parameters like Dasavidha parikshya,Astasthana parikshya 4-pulmonary function test and peak expiratory flow examinationTimepoint: oday,60 day an one during follow up

Primary

MeasureTime frame
1. Improvement in classical sign and symptoms of Tamaka Shwasa. 2.Decrease in frequency, duration and severity of attacks.Timepoint: 0 day,15th day,30th day,45th day60th day

Countries

India

Contacts

Public ContactDr Rajagopala Shrikrishna

All India Institute of Ayurveda

srajagopala@gmail.com7600902564

Outcome results

None listed

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