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A study to assess the use of intralesional Injection MMR in patients with molluscum contagiosum

To elucidate the therapeutic efficacy of intralesional injection Measles, Mumps and Rubella (MMR) vaccine in molluscum contagiosum - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/073075
Enrollment
42
Registered
2024-08-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: B081- Molluscum contagiosum

Interventions

Intervention1: injection MMR vaccine in molluscum contagiosum: Injection MMR 0.2ml will be injected into the largest lesion. The injections will be administered at 2-week intervals until complete clea

Sponsors

All Institute of Medical Sciences Bathinda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All consecutive untreated patients of molluscum contagiosum 2. Patients above 18 years of age 3. MC lesions more than 5

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating females. 2. Any evidence of immunosuppression, including HIV or family history of severe immune dysfunction. 3. With a prior history of hypersensitivity to Injection MMR 4. Patients having any significant systemic illness/ severe organ dysfunction or any sign of local infection.

Design outcomes

Primary

MeasureTime frame
Proportion of patients showing complete clearance of molluscum contagiosum lesions at 12 weeks follow up.Timepoint: Proportion of patients showing complete clearance of molluscum contagiosum lesions at 12 weeks follow up.

Secondary

MeasureTime frame
patients’ global assessment perceptions scoring at the end of treatment and at 24 weeks Score 1: Very much improved Score 2: Much improved Score 3: Minimally improved Score 4: No improvement Score 5: Minimal worse Score 6: Much worse Score 7: very much worse 2. The patient will be evaluated for any adverse effects and will be documentedTimepoint: Baseline, 2weeks, 4 weeks, 6 weeks, 8 weeks,12 weeks(4 weeks after last injection), 24 weeks(12 weeks after last injection)

Countries

India

Contacts

Public ContactKavita Poonia

AIIMS BATHINDA

kavitapoonia777@gmail.com09646091743

Outcome results

None listed

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