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Recruiting NCT07345897

NCT07345897 Emergency Department-based Cervical Cancer Screening Through Self-sampling

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Clinical Trial Summary
NCT ID NCT07345897
Status Recruiting
Phase —
Sponsor University of Rochester
Condition HPV
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2026-02-13
Primary Completion 2027-08

Eligibility & Interventions

Sex Female only
Min Age 30 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Cervical Cancer Screening

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 200 participants in total. It began in 2026-02-13 with a primary completion date of 2027-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

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

Contact & Investigator

Central Contact

Research Administrator

✉ peter_macdowell@urmc.rochester.edu

📞 585-274-1509

Frequently Asked Questions

Who can join the NCT07345897 clinical trial?

This trial is open to female participants only, aged 30 Years or older, up to 65 Years, studying HPV. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07345897 currently recruiting?

Yes, NCT07345897 is actively recruiting participants. Contact the research team at peter_macdowell@urmc.rochester.edu for enrollment information.

Where is the NCT07345897 trial being conducted?

This trial is being conducted at Rochester, United States.

Who is sponsoring the NCT07345897 clinical trial?

NCT07345897 is sponsored by University of Rochester. The trial plans to enroll 200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology