Acceptability of Testing DNA Markers in Vaginal Fluid for the Detection of Endometrial Cancer

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age45+
SponsorMayo Clinic

About this trial

This study evaluates how women feel about using DNA from a vaginal fluid collection for early detection of endometrial cancer.

Eligibility criteria

Qualifiers

Self-identified Black individuals ≥ 45 years with an intact uterus

Assigned female sex at birth

Willing to participate in a 30-minute virtual interview

Disqualifiers

Previous or current diagnosis of endometrial cancer

Trial design

Treatments tested in this trial

  • Non-Interventional Study

Treatment groups

25 Participants
are divided into 1 treatment group

Sponsors and collaborators