Status:

UNKNOWN

Efficacy of Intralesional MMR Vaccine,Intralesional Candidal Antigen&Topical Podophyllin in Treatment of Genital Warts

Lead Sponsor:

Assiut University

Conditions:

Condylomata Acuminata

Eligibility:

All Genders

3-50 years

Phase:

PHASE3

Brief Summary

This study compares the safety and efficacy of intralesional Candidal antigen versus Intralesional MMR vaccine versus podophyllin for treatment of genital warts.

Detailed Description

Anogenital human papillomavirus (HPV) is a highly prevalent sexually transmitted infection ,seen predominantly in young adults. Condyloma acuminata or benign anogenital warts are typically caused by ...

Eligibility Criteria

Inclusion

  • Patients with anogenital warts with ages ranging from 3 to 50 years
  • Genital warts resistant to treatment
  • Genital warts that had relapsed at least once after treatment with any of the tissue-destructive modalities.

Exclusion

  • Patients with any evidence of immunosuppression
  • Eczematous skin disorder
  • Those with any history of hypersensitivity to Candida albicans antigen
  • Pregnant or lactating women.

Key Trial Info

Start Date :

February 1 2020

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 1 2021

Estimated Enrollment :

45 Patients enrolled

Trial Details

Trial ID

NCT03853785

Start Date

February 1 2020

End Date

December 1 2021

Last Update

March 12 2019

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Efficacy of Intralesional MMR Vaccine,Intralesional Candidal Antigen&Topical Podophyllin in Treatment of Genital Warts | DecenTrialz