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Emergency Department-based Cervical Cancer Screening Through Self-sampling
RecruitingHealthy volunteers welcome
Advancing Cervical Cancer Screening Through Emergency Department-based Self-Sampling
Who can join
Ages 30 to 65 · Women · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Cisgender women and transgender/non-binary individuals with a cervix, * Age 30 - 65 years, and demonstrating decisional capacity to consent to participate with no known exclusion criteria present. Exclusion Criteria: * Past hysterectomy with cervical removal * Known infection with HIV (as screening recommendations for people with HIV differ from the general population) * Inability to consent (e.g., lacking decisional capacity, intoxicated, or in distress) * Current pregnancy or in the three months after giving birth * Use of vaginal ovules, creams or washes, vaginal contraceptives or condoms within past 3 days * Sexual intercourse or transvaginal ultrasound scans or gynecological examinations within past 2 days
About the study
This project will compare the uptake of cervical cancer screening through ED HPV sampling among patients presenting to the ED.
What is being tested
- Cervical Cancer Screening (diagnostic test)
Sponsor: University of Rochester · Participants: 200 · Started: Feb 13, 2026
Contact the study team
- Research Administrator · Phone: 585-274-1509
Official record on ClinicalTrials.gov — NCT07345897
Locations in the U.S.
| New York | University of Rochester Strong Memorial Hospital, Rochester |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.