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Clinical Trial to test the effectiveness of siddha medicine Amukkara Chooranam (Internal) & Sangamver Thailam (External) for the disease Venpulli (Vitiligo) in childre

Phase 2
Completed
Conditions
Health Condition 1: L80- Vitiligo
Registration Number
CTRI/2023/07/055194
Lead Sponsor
ational Institute of Siddha
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
30
Inclusion Criteria

Children of both sex in the age group of 5to 12 years with symptoms of hypo pigmented patches without any structural changes in any part of the body

Patient’s parent/ informant willing to sign the informed consent stating that he/she will consciously stick to the treatment during 60 days but can opt out of the trial of his/her own conscious discretion

Willing to cooperate for taking photographs whenever required with his/her consent

Exclusion Criteria

Albinism

Leprosy

Burns

scar

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Effectiveness of the trial drug is measured by VETI ScoreTimepoint: 60 days
Secondary Outcome Measures
NameTimeMethod
ILTimepoint: NI
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