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Clinical Trial Summary

The purpose of this study is to see the effects of two different standard of care treatments of endometrial cancer on sexual dysfunction. This study will compare two standard of care treatments: HDR (high dose radiation) vaginal brachytherapy 3 fractions of 7 Gy to HDR vaginal brachytherapy 6 fractions of 4Gy for early stage endometrial cancer.


Clinical Trial Description

Patients are randomized to HDR vaginal brachytherapy 7 Gy in 3 fractions prescribed at 5mm. Radiation delivered 4-12 weeks after surgery OR HDR vaginal brachytherapy 4Gy in 6 fractions prescribed at the cylinder surface. Patients have the option to request to decline their randomization and switch to the alternate treatment ARM if they prefer. Radiation delivered 4-12 weeks after surgery. Participants in all Arms will receive standard vaginal dilator for use after treatment (to promote healing). 3 month, 1 year and 2 year follow up assessments are performed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03785288
Study type Interventional
Source University of Virginia
Contact Song Wood
Phone 434-243-0008
Email UVARADONCClinicalTrials@uvahealth.org
Status Recruiting
Phase Phase 3
Start date January 17, 2019
Completion date January 1, 2026

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