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Screening Study for Cervical Pre-cancer and Cancer Prevention in South African Women.

Primary HPV Screening as an Indicator of Cervical Pre-invasive and Invasive Neoplasia in HIV-positive and -Negative Southern African Women

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02956031
Acronym
DiaVACCS
Enrollment
1500
Registered
2016-11-04
Start date
2016-12-31
Completion date
2038-12-31
Last updated
2025-07-08

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

Conditions

Cervical Cancer, High Grade Sil, CIN2

Keywords

cancer prevention, cervical screening, cervical cancer, cervical disease, cervical neoplasm, HPV testing, immunocytochemistry, triage techniques

Brief summary

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.

Interventions

OTHERScreening

Cervical specimen obtained using speculum examination and cervical collection bush.

OTHERColposcopy

Vaginal speculum examination followed by application of 2% acetic acid and lugol's iodine with inspection with colposcope and punch biopsies taken of abnormal areas.

PROCEDURELLETZ

The above (see colposcopy) is followed by local anaesthetic with two dentist's ampoules of lignocaine and large loop excision using coagulation of the abnormal area (usually 2 x 3 x 1 cm).

Sponsors

University of Stellenbosch
CollaboratorOTHER
University of Pretoria
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Informed consent accepted and signed * Health seeking behaviour or request for a cervical cancer screening test * Willing and able to receive test result by automated text message or clinic visit

Exclusion criteria

* Current pregnancy * Hysterectomy * Current or previous treatment for gynaecological cancer * Hesitant or unable to undergo screening and treatment if indicated

Design outcomes

Primary

MeasureTime frame
Number of women with histologically proven cervical intraepithelial neoplasia grade 2+ (CIN2+) detected using HPV DNA analysis with partial genotyping as primary screen test followed by cervical cytology and immunocytochemistry as triage testsDetected on histology biopsy at colposcopy after initial HPV screening with simultaneous cytology and immunocytochemistry testing

Secondary

MeasureTime frame
Number of women with CIN2+ detected using HPV DNA analysis with partial genotyping that is associated with HPV types 16, 18, 16 and/or 18, only other high risk typesDetected on histology biopsy at colposcopy after initial HPV screening with simultaneous cytology and immunocytochemistry testing

Countries

South Africa

Contacts

Primary ContactGreta Dreyer, PhD
greta.dreyer@up.ac.za+(27) 12 354 3900
Backup ContactCathy Visser, MSc
cathy.visser@up.ac.za+(27) 12 354 3900

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026