Rochester, NYNCT07345897Now EnrollingIRB Ready

HPV Clinical Trial in Rochester, NY

Access cutting-edge hpv treatment through this clinical trial at a research site in Rochester. Study-provided care at no cost to qualified participants.

Sponsored by University of Rochester

Quick Self-Assessment

See if you qualify for this Rochester location

Preparing your pre-screening questions…

Expert Care in Rochester

Access hpv specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related hpv treatment provided free

Apply for This Rochester Location

Check if you qualify for this hpv clinical trial in Rochester, NY

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Rochester

    Convenient for NY residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Rochester site if eligible
  4. 4Begin participation

About This HPV Study in Rochester

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

Sponsor: University of Rochester

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

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Rochester?

Yes, this clinical trial (NCT07345897) has an active research site in Rochester, NY that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

HPV Treatment Options in Rochester, NY

If you're searching for hpv treatment options in Rochester, NY, this clinical trial (NCT07345897) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Rochester research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hpv specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all hpv clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Rochester, NY