About this trial
This clinical trial aims to compare the efficacy and safety of intralesional acyclovir versus intralesional zinc sulphate in the treatment of plantar warts.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients aged 18-50 years of both sexes clinically diagnosed with multiple plantar warts.
Disqualifiers
Patients with wart types other than plantar warts (genital, common, and plane warts).
Pregnant or lactating women.
Immunocompromised patients.
Individuals receiving systemic immunosuppressive or antiviral therapy.
Trial design
Parallel
Treatments tested in this trial
Intralesional Acyclovir
DrugIntralesional injection of acyclovir, prepared using 250 mg acyclovir vial diluted with 3.5 ml saline (yielding an acyclovir concentration of approximately 70 mg/ml), at a dose of (0.1- 0.3 ml) injected into the largest (target) wart under aseptic precautions using an insulin syringe. The injection will be repeated every 2 weeks until complete clearance of warts or for a maximum of five sessions.
Intralesional Zinc Sulphate
DrugIntralesional injection of 2% zinc sulphate prepared using 2 gm of zinc sulphate powder dissolved in 100 ml of sterile distilled water and autoclaved at 95°C for 20 minutes, at a dose of (0.1- 0.3 ml) in the base of the largest (target) wart . The wart is injected with the solution till blanching or bleb formation. Subcutaneous injections and acral parts such as fingers and toes will be avoided, as it may cause vascular necrosis. Injections will be repeated for all patients into the same lesion every 2 weeks until complete clearance of warts or for a maximum of five sessions.
Treatment groups
Trial outcomes
Primary outcomes
Clinical Response of the Injected Warts
Clinical response assessed by standardized digital photographs and dermoscopic evaluation. Response will be graded using scoring system : Score 0: neither clinical nor dermoscopic response. Score 1: clinical improvement without dermoscopic clearance. Score 2: clinical disappearance with dermoscopic evidence of residual wart tissue. Score 3: complete clinical and dermoscopic clearance with return of normal skin markings.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: