Endometrial Cancer Clinical Trials

Find Endometrial Cancer Clinical Trials Near You

The ENDOMETRIAL Study: 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

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Diagnostic test
Study Type: Observational
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.

Eligibility
Participation Requirements
Sex: Female
Healthy Volunteers: f
View:

• Postmenopausal bleeding (defined as vaginal bleeding after absence of periods for ≥ 12 months) undergoing diagnostic evaluation for EC at gynaecological departments

• Treated in Central Denmark Region or Southern Denmark Region, Denmark

• Able to provide written consent for participation

• Able to read and understand Danish

Locations
Other Locations
Denmark
Department of Obstetrics and Gynaecology, Aarhus University Hospital
RECRUITING
Aarhus N
Department of Obstetrics and Gynaecology, Odense University Hospital
RECRUITING
Odense
Department of Obstetrics and Gynaecology, Randers Regional Hospital
NOT_YET_RECRUITING
Randers
Contact Information
Primary
Karen O. Binderup
kabind@rm.dk
+4524656562
Backup
Mette Tranberg, PhD
mettrani@rm.dk
+4578420264
Time Frame
Start Date: 2026-02-24
Estimated Completion Date: 2030-02-24
Participants
Target number of participants: 600
Treatments
Women with postmenopausal bleeding
Women referred for diagnostic evaluation to gynaecological departments for endometrial cancer due to postmenopausal bleeding
Related Therapeutic Areas
Sponsors
Collaborators: University of Southern Denmark, Region of Southern Denmark, Central Denmark Region, Randers Regional Hospital, Amsterdam UMC, Aarhus University Hospital
Leads: University of Aarhus

This content was sourced from clinicaltrials.gov