Non-Invasive Identification of Endometrial Cancer/Endometrial Atypical Hyperplasia With an AI-Based Classifier Applied to Transvaginal Ultrasound in Patients With Post-Menopausal Bleeding

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age55+
SponsorMayo Clinic

About this trial

This study evaluates if AI can be used with transvaginal ultrasound images for early detection of endometrial cancer or premalignant lesions.

Eligibility criteria

Qualifiers

Age ≥ 55 years

At least one episode of postmenopausal bleeding (PMB)

Endometrial biopsy available from at Mayo Clinic (MN, AZ, FL), Mayo Clinic Health System (MCHS), or an external institution

Acceptance to participate in the study

Disqualifiers

Diagnostic tests performed more than 90 days apart

Physical impediment/refusal to undergo transvaginal ultrasound (TVUS)

Trial design

Treatments tested in this trial

  • Non-Interventional Study

Treatment groups

300 Participants
are divided into 1 treatment group

Sponsors and collaborators