Clin2
NCT07214584Likely a fitRecruiting

Using blood and cervical tests to track cervical cancer treatment response

Cervical CancerHuman Papilloma Virus (HPV)

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

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.

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

Phase
N/A
Enrollment
55 people
Ages
18 years to 89 years
Study type
Observational

Who can take part

  • You are 18 years or older
  • You have cervical cancer linked to HPV (squamous cell, adenocarcinoma, or adenosquamous type)
  • Your cancer is stage I or higher, or has spread to other parts of the body
  • You have a tumor that can be seen on imaging scans, and you will have follow-up scans after treatment
  • You agree to give blood samples and cervical mucus samples for this study

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.

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