About this trial
This study looks at how well multiparametric ultrasound (mpUS) can assess vaginal tissue in women undergoing a specific treatment called intravaginal brachytherapy (IVRT) for endometrial cancer. IVRT is a common treatment, but it may cause some changes or discomfort in the vaginal area. Researchers want to see if mpUS imaging can help understand these effects better and if participants can tolerate the imaging process.
The trial's ID number is NCT07318415. It is not FDA-regulated and aims to include around 10 participants.
Who can join
Women aged 18 and older with a diagnosis of endometrial cancer can join. They should have had specific surgeries and be able to start radiotherapy within 12 weeks after surgery. Women cannot participate if they are receiving chemotherapy, have certain other health issues, or have had prior pelvic radiotherapy.
Condition
Endometrial Cancer
Age group
Adult, Older adult
The study team makes the final call on eligibility.
What happens in the study
All participants will receive standard IVRT and undergo mpUS imaging at several points: before treatment, right after treatment, and at 3, 6, and 12 months after treatment. They will also complete a questionnaire about their vaginal health.
Where
This trial is running at 7 locations in the United States. All of them are currently recruiting.
Memorial Sloan Kettering at Basking Ridge (Consent Only)
Basking Ridge, New Jersey
Memorial Sloan Kettering Bergen (Consent Only)
Montvale, New Jersey
Memorial Sloan Kettering Cancer Center
New York, New York
Memorial Sloan Kettering Monmouth (Consent Only)
Middletown, New Jersey
Memorial Sloan Kettering Nassau (Consent Only)
Uniondale, New York
Memorial Sloan Kettering Suffolk - Commack (Consent Only)
Commack, New York
Memorial Sloan Kettering Westchester (Consent Only)
Harrison, New York