Skip to content

Effect of Agastyaharitaki Avleha and granules in Shwasa

Pharmaceutical standardization of Agastyahareetaki Avaleha and Agastyahareetaki Granules and their comparative efficacy in the management of Tamaka Shwasa (Bronchial Asthma)

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/01/011419
Enrollment
60
Registered
2018-01-18
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: null- difficulty in breathing, cough, wheezing and chest tightness

Interventions

Intervention1: Group A: Treated with Agatyaharitaki Avaleha 6 gram of the drug twice a daily for 60 days before meal Control Intervention1: Group B: Treated with Agastyaharitaki granules 6 gram of the

Sponsors

Institute For Post Gradute Teaching and Research in Ayurveda Gujrat Ayurved University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Mild persistent cases of Bronchial Asthma with day time symptoms 3-6/week and nocturnal symptoms with 3-4/month. 2. 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: 1. Known patients of diabetes mellitus and uncontrolled HTN. 2. Dyspnoea resulting from cardiac origin, other lung pathologies (like-lower respiratory tract infection,Chronic obstructive pulmonary disease, Emphysema, upper respiratory tract obstruction, bronchiectasis,interstitial lung disease, occupational lung disease,tropical pulmonary eosinophilia,Tuberculosis, Pulmonary malignancy, chronic pluritis, plural effusion),anaemia. 3. Age above 60 years and below 16 years. Pregnant and lactating mothers. Patients suffering with other types of Shwasa,i.e. Maha, Urdha, ChhinnaShwasa will be excluded from the study. 4. Febrile patients on presentation or history of fever within past one week.

Design outcomes

Primary

MeasureTime frame
It is expected that the trial drugs will exert a significant action over Tamaka Shwasa (Bronchial Asthma)Timepoint: 2 month

Secondary

MeasureTime frame
significant relief in the sign and symptoms of tamaka shwasa (bronchial asthama)Timepoint: 2 month

Countries

India

Contacts

Public ContactVasundhra Jaluthriya

IPGT and RA

Patgiri124@gmail.com9426947438

Outcome results

None listed

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