MedTrace Logo

Oral Stent Device for Radiation Treatments of Oral Cancers

NCT04041141 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2021-02-09

No results posted yet for this study

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.

Conditions

  • Tongue Tumor
  • Tongue Cancer

Interventions

DIAGNOSTIC_TEST

CT Scan

An additional cone beam CT will be repeated at midcourse of therapy (3rd week) and during the end of therapy (5th week)

DEVICE

Experimental Oral Stent Device

Patients undergoing standard of care planning for head and neck tongue cancer will have a radiation plan of the body imaged via CT scan construction with the experimental oral stent device in place

Sponsors & Collaborators

  • Indiana University

    lead OTHER

Principal Investigators

  • Mark Langer, MD · Indiana University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-25
Primary Completion
2021-02-03
Completion
2021-02-03

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04041141 on ClinicalTrials.gov