Skip to main content
Evidence-Based Supplement Research
Evidence-Based Supplement Research

The efficacy of intralesional vitamin D3 injection in the treatment of cutaneous warts: A clinical therapeutic trial study.

  • 2023-08
  • Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) 29(8)
    • Haider Al-Sabak
    • Mohammed Al-Hattab
    • Marwah Al-Rammahi
    • Muhsin Al-Dhalimi

Study Design

Type
Clinical Trial
Sample size
n = 204
Population
40 patients (14 men and 26 females) with 204 cutaneous warts
Methods
Intralesional injection of vitamin D3 solution (600,000 IU) at 0.2 mL per patient, up to 5 warts per session, every 2 weeks for a total of four times; patients instructed to forego any topical or oral medication
Blinding
Open-label
Duration
every 2 weeks for a total of four times
  • Large Human Trial

Background

The human papillomavirus that causes warts is usually harmless, and it can infect any part of the skin or mucous membranes. Despite the availability of several treatments, warts often return, and scarring, pigmentation changes, and recurrence are all possible side effects.

Aim

Intralesional vitamin D3 was employed as an immunotherapy for cutaneous warts in the current investigation.

Materials and methods

In Al-Sadr Medical City in the city of Al-Najaf Al-Ashraf, a skin clinic conducted a therapeutic clinical experiment. A total of 204 cutaneous warts were examined in 40 patients (14 men and 26 females). Vitamin D3 solution of the dose (600 000 IU) was injected into the lesions' bases, with 0.2 mL per patient. Each session could only inject up to five warts. The injections were given every 2 weeks for a total of four times. Instructing patients to forego the use of any topical or oral medication was also a part of the protocol. Each patient was evaluated for recurrence risk before each therapy and then again 6 months later.

Result and discussion

There was a wide range of patient ages in this study, from 20 months to 52 years. About 65% of the cases included females. When looking at the many kinds of warts, the most prevalent was the common wart (71.6%). After four treatments, a positive response was considered to have occurred when all lesions had disappeared, a partial response when more than half of the lesions had disappeared, and no reaction when less than half of the lesions had disappeared. The final tally was 81.9% for those who responded in whole, 11.3% for those who responded partially, and 6.9% for those who did not respond at all. Next-session complete response rates were 12.7%, 29.9%, 54.9%, and 81.9%, respectively. Thirteen people experienced adverse symptoms, most noticeably minor swelling and itching. Within 6 months of follow-up, warts had completely disappeared for all patients with a partial or modest response except one who had no reaction.

Conclusion

Vitamin D3 administered intralesional is an effective and low-cost treatment for cutaneous warts.

Research Insights

  • 11.3% for those who responded partially

    Effect
    Beneficial
    Effect size
    Small
    Dose
    600,000 IU per session injected intralesionally every 2 weeks for 4 sessions
  • Within 6 months of follow-up, warts had completely disappeared for all patients with a partial or modest response except one who had no reaction

    Effect
    Beneficial
    Effect size
    Large
    Dose
    600,000 IU per session injected intralesionally every 2 weeks for 4 sessions
  • The final tally was 81.9% for those who responded in whole

    Effect
    Beneficial
    Effect size
    Large
    Dose
    600,000 IU per session injected intralesionally every 2 weeks for 4 sessions

Adverse Events Reported

  • Vitamin D3itching

    Thirteen people experienced adverse symptoms, most noticeably minor swelling and itching.

    Finding
    Reported
    Grade
    mild
  • Vitamin D3swelling

    Thirteen people experienced adverse symptoms, most noticeably minor swelling and itching.

    Finding
    Reported
    Grade
    mild
Back to top