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Clinical Trial Summary

Cervical cancer occurs commonly in HIV-infected women in South Africa. These women have poor response to treatment of cervical cancer precursors. This study will test whether giving the quadrivalent vaccine to women prior to surgical treatment of the cervical cancer precursor will improve outcomes. We hypothesize that pre-treatment HPV vaccine will result in a reduced occurrence or cervical cancer precursors in follow-up.


Clinical Trial Description

This is a single-center, randomized, double-blinded, placebo-controlled, phase II trial of the quadrivalent human papillomavirus vaccine (qHPV) in HIV-infected women to prevent occurrence of cervical HSIL after LEEP/LLETZ. Participants will undergo colposcopy with directed biopsies, cervical cytology, and stored HPV testing prior to vaccination. Participants will be randomized to the quadrivalent vaccine or saline placebo to be given at entry, week 4, and week 26. Women will have LEEP treatment at week 4. Participants will be seen in follow-up for cervical cytology, colposcopy with directed biopsies at weeks 26 and 52, and stored HPV specimens. Treatment assignment will be unblinded after study follow-up is completed for the last study participant. Women aged 45 or less randomized to placebo will be offered open label HPV vaccine after the study is concluded.. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01928225
Study type Interventional
Source University of Witwatersrand, South Africa
Contact
Status Completed
Phase Phase 2
Start date September 2, 2014
Completion date March 1, 2018

See also
  Status Clinical Trial Phase
Completed NCT03185013 - REVEAL 1 (Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL) Phase 3
Recruiting NCT05405270 - Predicting Response In Cervical Intraepithelial Neoplasia to Topical Imiquimod Treatment
Recruiting NCT06002126 - Optimization of Cervical Cancer Screening Among Women Living With HIV in Latin American Countries N/A
Completed NCT03721978 - REVEAL 2 Trial (Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL) Phase 3