Actively Recruiting

Phase 2
Age: 9Years +
All Genders
NCT05291845

Candida Antigen and Bivalent HPV Vaccine in the Treatment of Multiple Warts

Led by Zagazig University · Updated on 2025-06-12

162

Participants Needed

1

Research Sites

191 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To follow up the efficacy and safety of Candida antigen, bivalent HPV vaccine in treatment of common warts either mono or combined intralesional therapy

CONDITIONS

Official Title

Candida Antigen and Bivalent HPV Vaccine in the Treatment of Multiple Warts

Who Can Participate

Age: 9Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with multiple, recalcitrant, or non-recalcitrant common warts at different sites, sizes, and durations
  • Patients may have distant lesions
  • Patients of any gender aged 9 years or older
Not Eligible

You will not qualify if you...

  • Pregnant females
  • Known hypersensitivity to Candida antigen or bivalent HPV vaccine

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Reham Essam

Zagazig, Al Sharqia, Egypt, 2543

Actively Recruiting

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Research Team

R

Reham Essam, MD

CONTACT

R

Reham Essam, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

TREATMENT

Number of Arms

3

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