RecruitingNCT06365905

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


Sponsor

Mayo Clinic

Enrollment

300 participants

Start Date

Mar 27, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

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


Eligibility

Sex: FEMALEMin Age: 55 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether an AI tool applied to a vaginal ultrasound can accurately identify endometrial cancer or a pre-cancerous condition (atypical hyperplasia) in women who have experienced post-menopausal bleeding, without needing invasive testing. **You may be eligible if...** - You are 55 years or older - You have experienced at least one episode of bleeding after menopause - You have had an endometrial biopsy performed at Mayo Clinic or an affiliated institution - You are willing to undergo a transvaginal ultrasound **You may NOT be eligible if...** - Your diagnostic tests were performed more than 90 days apart - You are unable or unwilling to undergo a transvaginal ultrasound Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERNon-Interventional Study

Non-Interventional Study


Locations(3)

Mayo Clinic in Arizona

Scottsdale, Arizona, United States

Mayo Clinic in Florida

Jacksonville, Florida, United States

Mayo Clinic in Rochester

Rochester, Minnesota, United States

View Full Details on ClinicalTrials.gov

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NCT06365905


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