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Long-Term Follow-Up of HPV FOCAL Participants
Sponsor: University of British Columbia
Summary
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.
Official title: Evaluation of CIN2+ Rates up to 120 Months After 48-Month Co-Testing (Long Term Follow up of HPV FOCAL Participants)
Key Details
Gender
FEMALE
Age Range
30 Years - 69 Years
Study Type
OBSERVATIONAL
Enrollment
1710
Start Date
2020-09-30
Completion Date
2024-12-31
Last Updated
2026-04-28
Healthy Volunteers
No
Conditions
Interventions
HPV and cytology co-testing (via Liquid based collection device)
Liquid-based cytology co-testing is a procedure in which that a cervical sample is taken, and can be co-tested for HPV and standard cytology at the same time. It is collected in the same way that a traditional Pap is collected
Locations (1)
Women's Health Research Institute
Vancouver, British Columbia, Canada