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Comparative analysis of efficacy between autoimplantation and intralesional MMR vaccine in viral warts

Phase 2
Conditions
Health Condition 1: - Health Condition 2: L088- Other specified local infections of the skin and subcutaneous tissue
Registration Number
CTRI/2024/02/062715
Lead Sponsor
KLEH Dr Prabhakar Kore Hospital and Medical Research Institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1)Patients more than 12 years of age with multiple warts less than 10 in number who are willing to participate in the study

Exclusion Criteria

1)Single wart

2)Pregnant or planning pregnancy in the next three months

3)Lactating women

4)Patients with local dermatological condition

5)Patients with apparent infection, immunosuppression, or are on immunosuppressive drugs, asthma, allergic skin disorders, meningitis or convulsions

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction in size of wart assessed by VAS scoring systemTimepoint: Baseline,3 weeks, 6 weeks, 9 weeks, 12 weeks
Secondary Outcome Measures
NameTimeMethod
To assess adverse reactions in Inralesional Injection MMR & AutoimplantationTimepoint: Baseline, 3 weeks, 6 weeks, 9 weeks, 12 weeks
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