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A clinical study to evaluate effects of herbal medicine (Shirishadi Agad) and ayurvedic procedure (Virechana Karma) in treatment of Santamaka Shwasa (allergic asthma).

Evaluating efficacy of Shirishadi Agad and Virechana Karma in the management of Santamaka Shwasa w.s.r. to Allergic Asthma- A comparative randomized open clinical trial.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/04/018405
Enrollment
30
Registered
2019-04-03
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: shirashadi agad 40 ml,BD,empty stomach for 1 month amalaki rasayan 5gm,BD,for 2 month: â?¢ Shirishadi Agad in the dose of 40 ml in the forms of decoction twice a day for 1 month. â?¢ Du

Sponsors

All India Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of allergic asthma presenting with Tamaka Shwasa lakshna Total serum IgE concentration greater than or equal to 30 and less than or equal to 700 Intenational units per millilitre at Visit 0 History of at least moderate persistent allergic asthma (consistent with Global Initiative for Asthma [GINA] guidelines of more than 1 year in duration on a stable asthma treatment regimen including inhaled corticosteroids for the preceding 4 weeks An FEV1 while withholding short acting beta agonists for at least 6 hours and long acting beta agonists for at least 12 hours, of greater than or equal to 75 percentage of the predicted value at Visit 0 Evidence of reversible airway obstruction, as defined by an increase in FEV1 of more than or equal to 12 percentage between 20 to 30 minutes after 4 puffs (or less at the discretion of the investigator) of inhaled short-acting beta-agonist administration at Visit 0 or within the preceding year Pre-specified level of nocturnal asthma symptoms Non-smoker for at least 1 year prior to Visit 0, with a smoking history of no more than 10 pack-years (that is 1 pack,20 cigarettes per day for 10 years)

Exclusion criteria

Exclusion criteria: History of intubation for asthma Asthma exacerbation requiring treatment with systemic steroids within the preceding 3 months Asthma exacerbation requiring treatment in an emergency department or a hospital admission in the preceding 6 months Upper respiratory tract infection or sinusitis within the preceding 4 weeks History of an anaphylactic allergic reaction History of treatment with immunotherapy to any allergen within past 3 years History of aspirin or non steroidal anti inflammatory drug (NSAID) related asthma patients could have been included in NSAIDs use was avoided for the duration of the study

Design outcomes

Primary

MeasureTime frame
Changes in Doshik Anshansa kalpna (changes in total Asthma symptom score)Timepoint: Thirty days

Secondary

MeasureTime frame
Reduction in IgE level. Non-allergic response on exposure of allergen. Absolute eosinophil count Overall Improvement in Quality of life. Improvement in Agni Bala, Deha Bala and Chetas Bala as per Ayurveda Timepoint: Thirty days

Countries

India

Contacts

Public ContactDr Prasanth Dharmarajan

All India Institute of Ayurveda

divyakajaria@gmail.com8826167515

Outcome results

None listed

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