Clinical Trial

PRIORITY Study in Cervical Cancer

Study acronym: PRIORITY
Not Yet Recruiting
View on ClinicalTrials.gov →
Summary
The PRIORITY study is a prospective, multicenter observational study designed to evaluate an integrated diagnostic model combining extended molecular self-sampling and digital colposcopy supported by telemedicine for the prioritization of women at risk of cervical cancer. The study aims to assess the diagnostic performance, concordance, and clinical utility of this integrated approach in real-world settings, as well as its impact on diagnostic timeliness and patient navigation across different levels of care. Participants will undergo standard-of-care evaluation, and data will be collected on molecular test results, colposcopic findings, diagnostic outcomes, and time intervals within the care pathway. No interventions are assigned as part of the study protocol. The findings are expected to inform scalable strategies to improve early detection and optimize diagnostic pathways for cervical cancer, particularly in settings with structural and geographic barriers to timely care.
Trial Details
NCT Number NCT07593066
Lead Sponsor Pontificia Universidad Catolica de Chile
Conditions Cervical Cancer, Cervical Intraepithelial Neoplasia, HPV Infection
Enrollment 700 participants
Start Date 2026-06-30
Primary Completion 2026-12-31 (estimated)
Study Completion 2026-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-05-18