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Clinical Trial Summary

This is a prospective multi-center randomized clinical trial designed to demonstrate that daily online adaptive radiotherapy with concomitant chemotherapy for stage III non-small cell lung cancer (NSCLC) will result in decreased acute respiratory and esophageal toxicity compared with non-adaptive radiotherapy with concomitant chemotherapy. The timepoint for this assessment will be 1 month following the end of radiotherapy 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 NCT05488626
Study type Interventional
Source Varian, a Siemens Healthineers Company
Contact
Status Active, not recruiting
Phase N/A
Start date October 20, 2022
Completion date December 2025

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