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Phase 4
Age: 12Years +
All Genders
ID07448844

Intralesional Therapies For Cutaneous Viral Warts A Comparative Analysis Of Vitamin D3 And Acyclovir

Led by Riphah International University · Updated on 2026-03-10

40

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This clinical trial studies whether injecting acyclovir or vitamin D3 directly into skin warts helps clear them in people aged 12 and older who have common, plantar, flat, or periungual warts. It aims to find out if either treatment leads to complete wart clearance by week 8, which treatment works better, and what side effects occur. The trial is a Phase 4 study comparing two treatment groups with 20 participants each. Participants receive injections of either acyclovir or vitamin D3 into the wart every two weeks for up to four sessions. The dose varies by wart size, with injections given at the start and repeated biweekly. Both treatments are delivered directly into the wart lesion. This comparison helps researchers evaluate the effectiveness and safety of these two intralesional therapies. During the study, participants will have photographs taken of their warts before treatment and at every visit. Clinic visits include measuring the size and number of warts. After treatment, participants are followed for up to three months to monitor wart recurrence and any side effects. The main outcome measured is wart clearance at week 8, with additional tracking of early recurrence, adverse effects, and number of treatment sessions needed.

CONDITIONS

Brief Title

Intralesional Therapies For Cutaneous Viral Warts: A Comparative Analysis Of Vitamin D3 And Acyclovir

Who Can Participate

Age: 12Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 12 years and above with clinically diagnosed cutaneous warts
  • Common, plantar, flat, or periungual warts
  • Both treatment-nafve patients and those with recalcitrant warts
Not Eligible

You will not qualify if you...

  • Pregnant or lactating women
  • Immunocompromised patients
  • Individuals with history of hypersensitivity to vitamin D3 or acyclovir
  • Individuals receiving systemic immunosuppressive or antiviral therapy
  • Patients with secondary infection at injection site
  • Patients who had received any topical or destructive treatment for wart in previous three months

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