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study to compare treatment options in for warts using MMR vaccine and vitamin D injection

A randomized single blind controlled trial comparing efficacy of intralesional vitamin D injection and MMR (measles, mumps, rubella) vaccine in treatment of warts - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056461
Enrollment
37
Registered
2023-08-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: B079- Viral wart, unspecified

Interventions

Intervention1: intralesional vitamin D injection and MMR (measles, mumps, rubella) vaccine: All Group A patients will receive intralesional injection of up to 0.5 mL of reconstituted MMR vaccine into
15mg/ml) in each session after injection of IL lignocaine with 31 G insulin syringe into the single largest wart. Amount of injection on each wart will depend on the size of each wart. The session wil

Sponsors

sushil kumar singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age >12 years of either sex 2. Not received any systemic or oral therapy for management of warts in the last 4 weeks. 3. Willing to give consent for inclusion. 4. Willing for 3 weekly follow up.

Exclusion criteria

Exclusion criteria: 1. Patients under any systemic or topical treatment of warts within the last four weeks. 2. Patients with a past history of an allergic response to MMR or any other vaccine or Vitamin D. 3. Immunosuppressed patients • Pregnancy and lactating women

Design outcomes

Primary

MeasureTime frame
The clinical improvement will be graded as a full response, an excellent response, a fair response, a poor response, or no response based on the patients and physicians global evaluation using a visual analogue scale score at each visit, with baseline clinical photographs serving as controls. After each treatment session, the immediate and delayed adverse effects of MMR vaccination.Timepoint: 3 weekly monitoring after each dose and follow up at 3 months.

Secondary

MeasureTime frame
1. To determine the frequency & location of warts in patients visiting the outpatient department of dermatology at CNMC, Kolkata. 2. To determine the adverse effects associated with intralesional injection of MMR and vitamin D. Timepoint: at three weekly visits

Countries

India

Contacts

Public ContactSUSHIL KUMAR SINGH

calcutta national medical college

dr_Abhishek_de@yahoo.co.in9903275551

Outcome results

None listed

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