Clin2
NCT07480902Possibly a fitRecruiting

Comparing two tests for cervical cancer detection

I) Atypical Squamous Cells of Undetermined Significance (ASC-US)II) Atypical Glandular Cells of Uncertain Significance (AGUS)III) Cervical Intraepithelial Neoplasia (CIN), CIN-1, CIN-2, CIN-3IV) Low-grade Squamous Intraepithelial Lesion (LSIL)V) High-grade Squamous Intraepithelial Lesion (HSIL)VI) Cervical Cancer

Part of Cancer, Women’s health & pregnancy clinical trials.

This trial compares a liquid-based cytology test with a molecular screening test to find early changes in the cervix that could lead to cancer. It may help you understand which test is better at detecting these changes before they become serious.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
558 people
Ages
18 years to 85 years
Study type
Interventional

Who can take part

  • You are generally healthy and between 18 and 85 years old.
  • You must not eat for at least 6 hours and no more than 12 hours before the test.
  • You need to avoid sexual activity for 24 hours before the study.
  • You cannot be pregnant or think you might be pregnant.
  • You have not had a hysterectomy (surgery to remove the uterus).
  • You are not currently on chemotherapy, radiation, or other cancer treatment.
  • You do not have HIV or hepatitis.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT06866392Not yet recruiting
New cervical cancer screening with light and DNA test

This study is testing a new, non-invasive way to screen for cervical cancer. It uses a photoelectric device and an epigenetic test done on a sample from your cervix. The goal is to find early signs of cancer more accurately than current methods.

NCT07281430Recruiting
HPV self-test for cervical cancer screening

This study tests if a self-collected sample for HPV testing works as well as standard colposcopy to prevent cervical cancer. If you've recently had an abnormal cervical cancer screening and need a colposcopy, this trial may be an option for you.

Birmingham, Alabama
NCT05385406Recruiting
HPV screening with different ways to check for cervical problems

This trial tests two cervical screening approaches to find early signs of HPV-related changes. It may help by improving how results are sorted into “needs follow-up” versus “routine care,” especially for women with different HPV patterns.

Dschang, Menoua
NCT07214584Recruiting
Using blood and cervical tests to track cervical cancer treatment response

This trial checks how well cervical cancer responds to surgery, radiation, and chemotherapy by measuring HPV DNA and RNA in blood and cervical mucus. It aims to improve monitoring during treatment.

Gainesville, Florida
NCT05774561Recruiting
Using blood tests to monitor HPV-related cancer treatment

This study checks whether “liquid biopsies” (blood tests that look for cancer-related signals) can help monitor how HPV-related cancers respond to treatment. It may help doctors spot changes earlier during care.

Olomouc
NCT05282095Recruiting
Study how HPV changes affect outcomes in CIN2

This study follows women with an early abnormal cervix cell change (CIN2/CIN2-3) to see how HPV DNA “integration” relates to whether the condition improves or worsens. It may help doctors better predict prognosis and guide safer monitoring, especially if you want to become pregnant.

Fuzhou, Fujian

Hear when a new I) Atypical Squamous Cells of Undetermined Significance (ASC-US) trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.