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Comparative Efficacy of Shirishavaleha (Poly Herbal Ayurvedic Formulation) on Bronchial Asthma

Anti asthamatic activity of Shirishavaleha

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/10/004083
Enrollment
100
Registered
2013-10-21
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: J45- Asthma Health Condition 2: J453- Mild persistent asthma Health Condition 3: null- Patients of both sexes of 16 to 60 years with symptoms of Bronchial Asthma will be enrolled into the study

Interventions

Intervention1: Shirishavaleha: Patients will receive 10 gm of Shirishavaleha twice a day for 28 days followed by lukewarm water as an adjuvant In case of emergency, appropriate Bronchodilators, Corti

Sponsors

Institute for Post Graduate Teaching and Research in Ayurveda
Lead Sponsor
Dept of AYSUH
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients suffering with Mild persistent cases of Bronchial Asthma with daytime symptoms 3-6/week and nocturnal symptoms with 3-4/month and Moderate persistence cases with daytime symptoms daily and nocturnal symptoms with one or more than one week but not more than 2 weeks

Exclusion criteria

Exclusion criteria: Known patients of diabetes, dyspnoea resulting from cardiac origin, anaemia, age above 60 years and below 12 years, tuberculosis, malignancy and other chronic debilitating diseases, and patients who depend on regular use of inhalers will be excluded from the study

Design outcomes

Primary

MeasureTime frame
Improvement in AEC and other haematological (TLC, DLC, Hb, AEC), Peak Expiratory Flow Rate and Breath Holding TimeTimepoint: Improvement in AEC and other haematological (TLC, DLC, Hb, AEC), Peak Expiratory Flow Rate and Breath Holding Time

Secondary

MeasureTime frame
Overall improvement in the disease condition, Quality of Life of the diseased. Based on the observations, the study may be recommended to be added into the Essential Drugs List of Dept. of AYUSH, New DelhiTimepoint: 18 Months of Trial

Countries

India

Contacts

Public ContactDr Galib

Institute for Post Graduate Teaching and Research in Ayurveda

galib14@yahoo.co.in

Outcome results

None listed

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