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Testing Urine for HPV to Screen for Cervical Cancer in Women With HIV

Checks whether urine samples can detect cervical cancer risk in women living with HIV.

Plain-language title generated from the registry record
Registry title: Urine HPV Testing for Cervical Cancer Screening Among Women Living With HIV in South Africa

Key facts

Where
Westdene, South AfricaSee the site

Where in South Africa

  • Clinical HIV Research Unit Temba Lethu Wing Helen Joseph HospitalWestdene, South AfricaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
UNC Lineberger Comprehensive Cancer Center
Trial code
NCT05413798
Record updated
30 September 2026
Original description
The purpose of this study explores the usefulness of urine samples for cervical cancer screening in human immunodeficiency virus (HIV)-infected women.Read full original descriptionShow less

Clinical Performance Validation of Urine HPV Testing for Cervical Cancer Screening Among Women Living With HIV in South Africa

The purpose of this study explores the usefulness of urine samples for cervical cancer screening in human immunodeficiency virus (HIV)-infected women.

Cervical cancer occurs when women are infected with the human papillomavirus (HPV), which can cause changes in the cells that lead to cervical precancer and, eventually, cervical cancer if untreated. However, urine HPV testing has not been well validated low- and middle-income country settings, with no data available to guide its use in HIV-infected women.

Inclusion: In order to participate in this study a subject must meet all of the eligibility criteria outlined below; Confirmed HIV-1 infection; Age 25 years and older; Be willing and able to provide written informed consent.

Exclusion: Have been screened for cervical cancer within the preceding year (365 days); Have an active sexually transmitted infection (STI; women may participate once treated); Have a history of cervical cancer; Pregnant or intend to become pregnant within 90 days of enrollment; Have a surgically absent cervix; have been vaccinated against HPV.

ClinicalTrials.gov NCT05413798