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Clinical Trial Summary

This is a single-arm, prospective, multi-center clinical trial designed to demonstrate that adaptive radiotherapy for locally advanced cervical cancer will translate into a decreased rate of acute gastrointestinal toxicity compared with the historically reported rate for non-adaptive intensity modulated radiation therapy (IMRT). The timepoint for this assessment will be at week 5 of external beam radiotherapy (EBRT) and will use the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05197881
Study type Interventional
Source Varian, a Siemens Healthineers Company
Contact Steve Kohlmyer, MS
Phone 12062760076
Email steve.kohlmyer@varian.com
Status Recruiting
Phase N/A
Start date May 3, 2022
Completion date May 2028