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A trial to study the efficacy of quadrivalent HPV vaccine in anogenital wart

Efficacy of intralesional and intramuscular quadrivalent HPV vaccine in treatment of genital warts

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053364
Enrollment
40
Registered
2023-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B078- Other viral warts

Interventions

Intervention1: Intralesional quadrivalent HPV vaccine: Quadrivalent HPV vaccine will be injected into the lesions at week 0, 4 and 12 weeks Control Intervention1: Intramuscular HPV vaccine: Intramuscu

Sponsors

Dr s.n medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient of all genders >8 years Signed informed consent form Confirmed clinical diagnosis of genital condylomata

Exclusion criteria

Exclusion criteria: Individuals who are pregnant or are planning to become pregnant Participant allergic to yeast and vaccine components Patient who have received prior human papilloma virus vaccine Subjects who are immunocompromised or are on immunosuppressive medications or on immunomodulatory agents will be excluded

Design outcomes

Primary

MeasureTime frame
Changes in wart number between week 0 and week 12 Change in mean size of genital condyloma between week 0 and week 12Timepoint: Changes in wart number between week 0 and week 12

Secondary

MeasureTime frame
Change in score of specific questionnaire for condyloma accuminata (CECA) Change in score of dermatology quality of life index (DLQI)Timepoint: Week 0 and Week 12

Countries

India

Contacts

Public ContactManju Lata Verma

Dr S.N medical College jodhpur

mnjltvrm87@gmail.com9460651674

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026