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Clinical Trial Summary

The purpose of this study is to examine that ability of the experimental oral stent device to reduce the volume of mandible receiving >55 Gy by 50%during radiation treatment as assessed duri radiation treatment planning. Patients will have CT scans at three time-points during their standard of care radiation treatment. During these visits patients will receive scans via CT or cone beam CT scan, with both the standard and experimental oral stent devices. During radiation treatment patients will receive the standard oral stent device.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04041141
Study type Observational
Source Indiana University
Contact
Status Withdrawn
Phase
Start date September 25, 2019
Completion date February 3, 2021

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