Emergency Department-based Cervical Cancer Screening Through Self-sampling
This project will compare the uptake of cervical cancer screening through ED HPV sampling among patients presenting to the ED.
| Condition(s) | HPV, HPV Associated Cancers, HPV Cancers, Cervical Cancer Screening, Cervical Cancer (Early Detection) |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | This project will compare the uptake of cervical cancer screening through ED HPV sampling among patients presenting to the ED. |
| Who can participate | 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 |
| Ages | 30 Years to 65 Years |
| Sex | Female |
| Accepts healthy volunteers | Yes |
| Lead sponsor | University of Rochester |
| Locations | Rochester, New York, United States |
| Start date | 2026-02-13 |
| NCT ID | NCT07345897 |
| Official listing | https://clinicaltrials.gov/study/NCT07345897 |