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RECRUITING
NCT05625633
PHASE2/PHASE3

Human Papillomavirus (HPV) Vaccination vs. Placebo for the Treatment of Refractory Cutaneous Warts

Sponsor: Western Institute for Veterans Research

View on ClinicalTrials.gov

Summary

This double-blinded clinical trial randomly assigns participants with refractory cutaneous warts to receive either treatment with the human papillomavirus (HPV) vaccine or a placebo to assess the efficacy of HPV vaccination for the treatment of refractory cutaneous warts.

Official title: Human Papillomavirus (HPV) Vaccination for the Treatment of Refractory Cutaneous Warts: A Randomized, Placebo-Controlled, Double-Blinded Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2024-03-25

Completion Date

2026-12

Last Updated

2024-04-05

Healthy Volunteers

No

Conditions

Interventions

BIOLOGICAL

Human Papillomavirus 9-valent Vaccine, Recombinant

0.5-mL suspension of 9-valent Gardasil administered as intramuscular injection at weeks 0, 4, and 20

OTHER

Normal Saline

0.5-mL normal saline administered as intramuscular injection at weeks 0, 4, and 20

Locations (2)

University of Utah Midvalley Health Center

Salt Lake City, Utah, United States

VA Salt Lake City Health Care System

Salt Lake City, Utah, United States