Human Papilloma Virus Genotypes and Treatment Outcomes of Intralesional Immunotherapy of Anogenital Warts
Human Papilloma Virus, Anogenital Wart
About this trial
This is an interventional treatment trial for Human Papilloma Virus
Eligibility Criteria
Inclusion Criteria: - Patients with clinically diagnosed multiple anogenital warts who had not received treatment in the last 2 months before the study Exclusion Criteria: Patient refusal, pregnancy, lactation, age less than 10 years, and immunosuppressive conditions
Sites / Locations
- Rana EhabRecruiting
Arms of the Study
Arm 1
Experimental
treatment group
All patients will be subjected to: A thorough history taking and proper dermatological examination. Skin sampling from anogenital wart lesions: skin sterilization followed by injection of local anesthesia at the base of lesions, then the part of wart above skin surface will be removed using shave biopsy technique. DNA extraction of skin samples. Conventional PCR for low-risk HPV genotypes (6,11) and RT-PCR for high-risk HPV genotypes. Intralesional injection of the quadrivalent HPV vaccine (Gardasil) at a dose of 0.5ml, into the largest wart at 4-week intervals until complete clearance is achieved or for a maximum of three sessions.