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To study the efficacy of tuvarakadi cream in the managment of eczema in children

Not yet recruiting
Conditions
Atopic dermatitis, unspecified. Ayurveda Condition: CARMADALA-KUSHTHAH,
Registration Number
CTRI/2025/04/085361
Lead Sponsor
Sane Guruji Arogya Kendra
Brief Summary

This is a clinical study to assess the efficacy of tuvrakadi cream in the management of charmadala in the age group of 6 months to 2 year children with special reference to atopic dermatitis

Primary objective is to study the effectiveness of tuvarakadi cream as bahirparimarjana in the management of charmadala in kshreerap and kshreeranada balak in the timespan of 14 days.

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

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Patient having classical signs and symptoms of Vataj Charmadala.
  • Infants and toddlers between the Age group 6 months to 2 years.
  • Patients irrespective of sex, religion and socioeconomical status.
  • Patient of the parent who will give written consent will be included.
Exclusion Criteria
  • Charmadala associated with sphota.
  • Patient with associated skin infections such as herpes simplex, herpes zoster, scabies, impetigo or lichen simplex chronicus and congenital syphilis.
  • Children having any other associated illness such as acute exacerbation of asthma or hey fever.
  • Children admitted in NICU and PICU.
  • Children receiving phototherapy.
  • Patient with more than 60 % body surface involvement.
  • Patient taking treatment from any other pathy for the same problem.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate efficacy of Tuvarakadi cream in the management of charmadalaTreatment will be given for 14 days | Tuvarakadi will be given to the patient for external application. | Follow up and assessment will be done after7th day and 14th day. | Final observation will be recorded after | completion of treatment.
in the age group of 6 months to 2 year old children in time span of 14 daysTreatment will be given for 14 days | Tuvarakadi will be given to the patient for external application. | Follow up and assessment will be done after7th day and 14th day. | Final observation will be recorded after | completion of treatment.
Secondary Outcome Measures
NameTimeMethod
To observe adverse effect & evaluate the safety of Tuvarakadi cream in the management of charmadala inthe age group of 6 months to 2 year old children in the time span of 14 days

Trial Locations

Locations (1)

Sane guruji arogya kendra

🇮🇳

Pune, MAHARASHTRA, India

Sane guruji arogya kendra
🇮🇳Pune, MAHARASHTRA, India
Dr Rashmi Meshram
Principal investigator
rashmimeshram99@gmail.com

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