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TO STUDY THE EFFECTIVENESS OF INTRALESIONAL MEASLES MUMPS RUBELLA VACCINE AND VIT D3 FOR THE TREATMENT OF WARTS

A Comparative Study To Evaluate The Efficacy Of Intralesional Measles, Mumps And Rubella Vaccine And Intralesional Vitamin D3 In The Treatment Of Extragenital Warts

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/09/027933
Enrollment
90
Registered
2020-09-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: L088- Other specified local infections of the skin and subcutaneous tissue

Interventions

Intervention1: A Comparative Study To Evaluate The Efficacy Of Intralesional Measles, Mumps And Rubella Vaccine And Intralesional Vitamin D3 In The Treatment Of Extragenital Warts: Our study is a rand

Sponsors

Dr Trisha Patel
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with clinically confirmed cases of all type of warts in age groups >2 years and <70 years included in the study.

Exclusion criteria

Exclusion criteria: 1) Immunocompromised patient such as patient taking anticancer drug, immunosuppressive drugs, steroids. 2) Patients with clinical history of immunosuppression. 3) Pregnant female (Married females in reproductive age group are excluded by UPT) and Lactating females, patient with generalized eczema, infective dermatosis, and patient with known hypersensitivity to Vit-D3 or MMR immunotherapy 4) Any acute illness/ acute febrile illness 5) Children less than 2 years 6) Patients with inflamed warts

Design outcomes

Primary

MeasureTime frame
Partial or complete resolution of the viral warts in majority of the casesTimepoint: The patient will be evaluated at the beginning of study and then at interval of 21 days for 4 time. After that patient will be followed up at the interval of 3 and 6 months to see for recurrence.

Secondary

MeasureTime frame
We will be able to evaluate the process of regression of the viral wartTimepoint: we will have an evaluation of disease activity at every 21 days and see for recurrence at the end of 6 months after the last injection

Countries

India

Contacts

Public ContactDr Trisha Patel

PRAMUKH SWAMI MEDICAL COLLEGE AND SHREE KRISHNA HOSPITAL

dr.trishapatel@gmail.com7990173791

Outcome results

None listed

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