Skip to main content
Clinical Trials/CTRI/2025/01/078967
CTRI/2025/01/078967Not yet recruitingNot Applicable

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

Sane Guruji Arogya Kendra1 site in 1 country60 target enrollmentStarted: January 30, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
60
Locations
1
Primary Endpoint
To evaluate efficacy of paushakaradi syrup and balchaturbhadra syrup in the management of kaphaj kasa in children of age group 5 to 10 years

Study Overview

Brief Summary

This is a comparative clinical study between the efficacy of paushkaradi syrup and balchaturbhadra syrup in the management of kaphaj kasa in children of age group 5-10 years

Primary objective is to compare efficacy of paushakaradi syrup and balchaturbhadra syrup orally for 7 consecutive days in kaphaj kasa in children with age group of 5 to 10 years

Assesment of signs and symptoms will be done and observation will be drawn from the outcome of patient

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
None

Eligibility Criteria

Ages
5.00 Year(s) to 10.00 Year(s) (—)
Sex
All

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

  • 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.

Outcomes

Primary Outcomes

To evaluate efficacy of paushakaradi syrup and balchaturbhadra syrup in the management of kaphaj kasa in children of age group 5 to 10 years

Time Frame: 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 Outcomes

  • literature study of kaphaj kasa in paediatric age group(to observe adverse effect if any)

Investigators

Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr Rutuja Ramchandra Patil

MAM S Sumatibhai Shah Ayurved Mahavidyalaya Malwadi Hadapsar Pune

Study Sites (1)

Loading locations...

Similar Trials