Intralesional Vitamin D3 Versus Intralesional Acyclovir in Treatment of Plantar Warts

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05324904
Collaborator
(none)
44
1
2
13
3.4

Study Details

Study Description

Brief Summary

To evaluate and compare the efficacy and safety of intralesional acyclovir versus intralesional vitamin D3 in the treatment of plantar warts

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Introduction Warts are common epidermal growths caused by various strains of human papillomavirus (HPV) affecting all age groups. They have an unsightly appearance and are mostly asymptomatic but sometimes may be painful as in the case of palmoplantar warts . Plantar warts is a clinical variant that occur on sole of the foot, most frequently over pressure points .

It is estimated that 40% of population is infected with HPV, and in 7% to 12%, a wart develops . Plantar warts exhibit an annual incidence of 14% in the general population . Sixty-five percent to 78% of cutaneous warts have been shown to regress within 2 years . In persons older than 12 years, the rate of spontaneous regression significantly decreases .

Variable therapeutic options are available for treating warts, with none considered a gold standard. Primary treatments include topical salicylic acid, topical imiquimod, topical 5-fluorouracil, cryotherapy, excision, electrocautry and laser vaporization .

Vitamin D is a fat-soluble steroid prohormone that has wide range of biological actions e.g. inhibition of cellular proliferation, induction of terminal differentiation, and inhibition of angiogenesis. It also stimulates macrophages and cathelicidin production . Recently, several studies have demonstrated the efficacy of intralesional vitamin D in treatment of warts, as well as recalcitrant lesions, with clearance rates of 72.5%-90% .

Acyclovir is a synthetic purine nucleoside analogue with activity against some viruses as herpes simplex and varicella-zoster virus. Acyclovir uses viral thymidine kinase to convert to its active form, acyclovir triphosphate. Through this mechanism of utilizing viral thymidine kinase, acyclovir specifically targets viral DNA preventing its replication in the host.

Previously, few studies and case reports documented the clearance of warts, some were unresponsive to prior treatment, with both topical and oral use of acyclovir .

A recent study has evaluated the efficacy of intralesional acyclovir versus intralesional saline in treatment of warts and reported complete clearance rate of 52.6% and a partial response of 16.7% for acyclovir with a statistically significant difference from saline (0% complete clearance) .

Study Design

Study Type:
Interventional
Anticipated Enrollment :
44 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Intralesional Vitamin D3 Versus Intralesional Acyclovir in Treatment of Plantar Warts
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Nov 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: group 1

this group will be intralesionaly injected with vitamin D3

Drug: Vitamin D
- Vitamin D The aqueous solution of vitamin D3 (cholecalciferol) will be used ampoule 200,000 IU/2 ML, Using a 27-gauge syringe with the bevel facing upward, a maximum of 0.6 ml (60,000 IU) of vitamin D3 solution will be slowly injected into the base of the largest plantar wart (large warts > 10 mm need multiple injections at different sites) Treatment sessions will be performed at 3-week intervals for a maximum of 4 sessions

Active Comparator: group 2

this group will be intralesionally injected with acyclovir

Drug: acyclovir
-Acyclovir Acyclovir vial (Zovirax® vial, 250mg, ) will be diluted with 3.5 ml saline to get approximately 70 mg /ml solution. After sterilization of the skin, a 27-gauge syringe with the bevel facing upward will be inserted into the base of the largest plantar wart to slowly inject the solution Treatment sessions will be performed at 2-week intervals for maximum of 5 sessions

Outcome Measures

Primary Outcome Measures

  1. complete healing rate [12 weeks]

    Main outcome variable is the complete healing rate among planter warts patients treated with intralesional vitamin D3 compared to those by Intralesional acyclovir

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult participants of both sex with plantar warts will be included in the study
Exclusion Criteria:
    • Children < 12 years.
  • Pregnant and lactating women.

  • Receiving any treatment for warts within 1 month before the study.

  • Systemic antiviral medication.

  • Previous history of vitamin D or acyclovir hypersensitivity.

  • Vitamin D supplementation.

  • Concurrent other skin disorders.

  • Immunosuppressive disorders or receiving immunosuppressive drugs.

  • Receiving drugs that may alter vitamin D level including prednisone, orlistat, phenytoin and thiazide diuretics.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Assuit University Assiut Egypt

Sponsors and Collaborators

  • Assiut University

Investigators

  • Principal Investigator: maha m mostafa, MD, Assuit University faculty of medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
maha mostafa ali mostafa, Resident physician of Dermatology, Venereology and Andrology, kom Ombo central hospital, Assiut University
ClinicalTrials.gov Identifier:
NCT05324904
Other Study ID Numbers:
  • vitamin D3, acyclovir in warts
First Posted:
Apr 13, 2022
Last Update Posted:
Apr 13, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 13, 2022