Sponsor
University of British Columbia
Status
Active, not recruiting
ClinicalTrials.gov ID
For more information, see ClinicalTrials.gov NCT04185389
This FOCAL follow-up study aims to assess the long-term effectiveness and safety of primary HPV testing for cervical cancer screening. A cohort of participants from the original FOCAL study will be asked to see their health care provider to submit another cervical sample for cytology and HPV testing. This will permit evaluation of long term safety and effectiveness of primary HPV testing up to ten years after a participant's first screening in the FOCAL study and comparison of primary HPV testing to HPV and cytology co-testing.
Intervention
HPV and cytology co-testing (via Liquid based collection device)
Condition
Cervical Cancer
Investigators
Gina Ogilvie, MD, MSc FCFP DrPH, Laurie Smith, MPH