Clinical Trial

Evaluation of DNA Methylation Markers for Endometrial Cancer Risk-stratification Using Patient-collected Urine and Vaginal Samples and Clinician-collected Cervical Samples From Women With Postmenopausal Bleeding

Recruiting
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Summary
The goal of this observational study is to investigate the clinical utility of DNA-methylation testing in urine and vaginal samples collected by patients and cervical samples collected by clinicians, to determine the risk of endometrial cancer in symptomatic women with postmenopausal bleeding. The study aims to answer the following research questions: * What is the diagnostic accuracy of DNA methylation testing in urine, vaginal and cervical samples compared to traditional TVUS for endometrial cancer detection? * What is the 2-year risk of EC among women testing negative on TVUS and/or DNA methylation tests or those testing positive on methylation only? Researchers will compare DNA methylation testing in patient-collected urine and vaginal samples as well as in clinician-collected cervical samples, with the traditional diagnostic pathway for women with PMB, which includes TVUS evaluation, and when indicated by abnormal TVUS findings, endometrial biopsy according to clinical guidelines. Participants will * take a urine and vaginal sample * have a cervical sample collected by a clinician * undergo TVUS evaluation according to clinical guidelines * If TVUS shows thickened endometrium (≥ 5 mm) and/or irregularity, an endometrial biopsy will be collected according to clinical guidelines * fill out a questionnaire regarding acceptability and preferences of sampling methods and complete a lifestyle questionnaire.
Protocol Amendment History 1 change
critical Trial status changed: Enrolling by Invitation → Recruiting 2026-05-14
Trial Details
NCT Number NCT07400835
Lead Sponsor University of Aarhus
Collaborators: Central Denmark Region, University of Southern Denmark, Randers Regional Hospital, Region of Southern Denmark, Amsterdam UMC, Aarhus University Hospital
Conditions Postmenopausal Bleeding
Enrollment 600 participants
Start Date 2026-02-24
Primary Completion 2028-02-24 (estimated)
Study Completion 2030-02-24 (estimated)
Updated on ClinicalTrials.gov 2026-05-13