HPV Testing for Postmenopausal Women

Screening Triage and Risk Stratification

Recruiting Observational Study
Cervix Cancer HPV Testing Postmenopausal Women
Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
23 – 64
Sex
Female
Study type
Observational
Participants needed
5,000 (estimated)
Sponsor
University of Aarhus · Other
Who this trial is looking for

This trial is looking for postmenopausal women aged 50-64 who have tested positive for HPV. Participants will undergo tests to help understand the risk of developing cervical issues over time.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am a woman aged 50-64 and tested positive for HPV.
  • I am a woman aged 23-64 who had a LEEP procedure and will undergo follow-up tests.

You may not be able to join if

  • I have rejected participation in research before.
  • I have an invalid HPV or cytology result six months after LEEP.
  • I have no residual material available for testing.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
* To investigate the performance of cytology, extended genotyping, p16/Ki67 dual stain cytology, DNA methylation and viral load as triage markers in post-menopausal HPV-screen-positive women aged 50-64 years in the organized screening program to predict the risk of developing CIN2+. (work package 1) * To investigate the performance of cytology, extended genotyping, p16/Ki67 dual stain cytology, DN…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * HPV-screen-positive (aged 50-64) * Women who undergo test-of-cure (i.e. HPV and cytology) six months after LEEP in Central Denmark Region (aged 23-64) * Women who undergo follow-up test (i.e. HPV and cytology) 12 months after LEEP * A valid cytology-triage result (aged 23-64) …
Contacts

mette tranberg, post doc

40113676

mettrani@rm.dk

CONTACT

Line Winther Gustafson, MD

+4578420264

Line.Winther@skejby.rm.dk

CONTACT