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Adjuvant VaccInation After Conization for the Treatment for CervicAL Dysplasia (VITAL)

F

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano

Status

Enrolling

Conditions

Cervical Intraepithelial Neoplasia

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

HPV vaccination has emerged as a strategy to reduce the risk of recurrence oafter excisional treatment. However, only few data are aviable. In this trial the investigators aim to assess the role of HPV vaccination in women traeted for HPV-related lesions

Full description

Patients treated for HPV-related disease are counseled about the potential protective role of HPV vaccination. The investigators will monitor the risk of HPV recurrence in pateints who choce to have vaccination and who did not.

Enrollment

600 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Treatment of HPV-related disease

Exclusion criteria

  • Previous HPV vaccination

Trial design

600 participants in 1 patient group

treatment of HPV-related disease with or without vaccination

Trial contacts and locations

1

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Central trial contact

Giorgio Bogani, ph.d.

Data sourced from clinicaltrials.gov

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