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To study the difference between the effect of the paushakardi syrup and balchaturbhadra syrup in the management of kaphaj kasa in children

A comparative clinical study between the efficacy of the paushakardi syrup and balchaturbhadra syrup in the management of kaphaj kasa in children of age group 5-10 years - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/078967
Enrollment
60
Registered
2025-01-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: J20- Acute bronchitis

Interventions

None listed

Sponsors

Sane Guruji Arogya Kendra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient having classical signs and symptoms of kaphaj kasa Mandagni Aruchi Pinasa Asyamadhurya Stivanayuktakasa, Swarabhed, Kanthekandu. Age group 5 yr to 10 yr Patients irrespective of sex religion and socioeconomical status Patient who give written consent will be included.

Exclusion criteria

Exclusion criteria: Kasa other than kaphaj kasa Kaphaj Kasa associated with jwara Patient with condition like known case of Pneumonia TB Bronchial Asthma Immunocompromised diseases like Juvenial Diabetes Mellitus will be excluded 4.Patient having any chronic and systemic illness.

Design outcomes

Primary

MeasureTime frame
To evaluate efficacy of paushakaradi syrup and balchaturbhadra syrup in the management of kaphaj kasa in children of age group 5 to 10 yearsTimepoint: Treatment will be given for 7 days Paushkaradi syrup will be given for one group and balchaturbhadra syrup will be given for another group . Follow up and assessment will be done after 3rd 5th and 7th day. Assessment will be done by objective and subjective parameters. Final observation will be recorded after completion of treatment—

Secondary

MeasureTime frame
literature study of kaphaj kasa in paediatric age group to observe adverse effect if anyTimepoint: Study will be done using Ayurvedic Granthas & modern texts Preparation of drugs will be done according to standard procedure During treatment observation will be done on 3rd 5th & 7th day & later adverse effect—

Countries

India

Contacts

Public ContactDr Ramchandra Pandurang Babar

MAM S Sumatibhai Shah Ayurved Mahavidyalaya Malwadi Hadapsar Pune

ramchandrababar@gmail.com8275459236

Outcome results

None listed

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