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)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06365905
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