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Difference in effect of oral isotretinoin in combination with intralesional MMR and intralesional MMR alone in extragenital cutaneous warts: A randomized clinical trial

Efficacy of oral isotretinoin with intralesional MMR vs intralesional MMR alone in extragenital cutaneous warts: A randomized clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069158
Enrollment
66
Registered
2024-06-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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: Efficacy of oral isotretinoin with intralesional MMR in extragenital cutaneous warts: Patients diagnosed with warts in age group of 14–60 years and having 5 or more warts will be inclu
group B will receive intralesional MMR alone. Treatment duration in both groups will be 12 weeks or until clinical resolution, whichever is earlier, and patients will be followed up for 1 month post-

Sponsors

AIIMS Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Clinical diagnosis of warts. 2. Patient having 5 or more warts. 3. Age 14 – 60 years. 4. No topical treatment in last 2 weeks and systemic treatment in previous 4 weeks.

Exclusion criteria

Exclusion criteria: 1. Known hypersensitivity to vaccine or its component or isotretinoin. 2. Pregnant and lactating female. 3. Known case of-HIV, hepatitis B, hepatitis C. 4. Immunocompromised patients. 5. Patient having chronic liver disease, kidney disease or systemic illness.

Design outcomes

Primary

MeasureTime frame
To compare efficacy of oral isotretinoin with intralesional MMR vs intralesional MMR alone in terms of:- 1. Grading of clearance of warts 2. Time needed for complete lesion clearance 3. The number of sessions needed for clearance of all warts completely.Timepoint: Baseline, 3 weeks, 6 weeks, 9 weeks, 12 weeks and 4 weeks post treatment

Secondary

MeasureTime frame
1. Recurrence rate 2. Patient satisfaction score 3. DLQI (Dermatology life quality index) 4. To compare side effects profile of two groups.Timepoint: Baseline, 3 weeks, 6 weeks, 9 weeks, 12 weeks and 4 weeks post treatment

Countries

India

Contacts

Public ContactSaurabh Kushwaha

AIIMS JODHPUR

doc.trinity@yahoo.com7297895727

Outcome results

None listed

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