Emergency Department-based Cervical Cancer Screening Through Self-sampling

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexFemale

Age30-65

SponsorUniversity of Rochester

About this trial

This project will compare the uptake of cervical cancer screening through ED HPV sampling among patients presenting to the ED.

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

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

200 Participants

are divided into 1 treatment group

University of Rochester Strong Memorial Hospital14642, RochesterNew York, United States

University of Rochester

Lead sponsor