Actively Recruiting
Screening Study for Cervical Pre-cancer and Cancer Prevention in South African Women.
Led by University of Pretoria · Updated on 2025-07-08
1500
Participants Needed
1
Research Sites
1147 weeks
Total Duration
On this page
Sponsors
U
University of Pretoria
Lead Sponsor
U
University of Stellenbosch
Collaborating Sponsor
AI-Summary
What this Trial Is About
Nearly 8 000 new cervical cancer cases are diagnosed in South Africa per year; many are still undiagnosed and about 50% of diagnosed cases succumb per year. Although the current prevalence of pre-cancer cervical disease is largely unknown, data from local studies suggest regional differences and an increase in the prevalence of cytological abnormalities when compared with historical data. Low frequency in cytology screening is the primary factor attributable to development of invasive cervical cancer and almost one-third of all cervical cancer patients had previous negative cytology. Due to the low sensitivity of cytology it can be assumed that the true prevalence of pre-cancer disease is underestimated by all available data. One round of optimal cervical cytology will detect around 50% of existing pre-cancer cervical disease as identified and proven using colposcopy and directed biopsy. It is now widely accepted that primary screening with a human papilloma virus (HPV) test can improve the sensitivity of screening and that even a single round of HPV screening can rapidly reduce the incidence of invasive cervical cancer and related mortality within a few years. South Africa has a high prevalence of HIV infection and a delay in or failure to initiate antiretroviral therapy (ART). These facts, together with the largely unscreened status of the female population and the high incidence of cervical cancer all suggest that HPV infection and precursors to cervical cancer are both unusually common among South African women. Accurate current knowledge of the performance of newer generation HPV based screening tests in HIV-infected and general female population are essential for cost-analysis and planning for national prevention and screening programs. This study will aim to demonstrate the feasibility and efficacy of new generation HPV deoxyribonucleic acid (DNA) based screening assays in a South African setting. The investigators hypothesize that HPV testing followed by normal and special cytology tests will be a successful screening model for a South African population.
CONDITIONS
Official Title
Screening Study for Cervical Pre-cancer and Cancer Prevention in South African Women.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent
- Seeking health care or requesting cervical cancer screening
- Willing and able to receive test results by text message or clinic visit
You will not qualify if you...
- Current pregnancy
- History of hysterectomy
- Current or previous treatment for gynecological cancer
- Unwilling or unable to undergo screening and treatment if needed
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Steve Biko Academic Hospital
Pretoria, Gauteng, South Africa
Actively Recruiting
Research Team
G
Greta Dreyer, PhD
CONTACT
C
Cathy Visser, MSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here