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Real-Time kV Imaging vs. Real-Time 3D Patient Surface Tracking for Head & Neck Cancer

This study has been terminated.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01011842
First Posted: November 11, 2009
Last Update Posted: May 27, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Varian Medical Systems
Information provided by (Responsible Party):
Quynh-Thu Le, Stanford University
November 9, 2009
November 11, 2009
May 27, 2015
October 2009
March 2010   (Final data collection date for primary outcome measure)
We are measuring how much a patient moves during treatment. [ Time Frame: This information will be available immediately have the patient is treated. ]
How much a patient moves during treatment. [ Time Frame: immediately after the patient is treated. ]
Complete list of historical versions of study NCT01011842 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
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Real-Time kV Imaging vs. Real-Time 3D Patient Surface Tracking for Head & Neck Cancer
Comparison of Intrafraction Motion in Patients With Head and Neck Cancer Using Real-Time kV Imaging vs. Real-Time 3D Patient Surface Tracking
To determine if a new optical system that can track a patient's movement during treatment can be used to measure motion and allow for motion adjustments in order to decrease the amount of healthy tissue that receives radiation without limiting our ability to cure cancers using radiation.
Not Provided
Interventional
Not Provided
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Head and Neck Cancer
  • Procedure: Radiotherapy
    Standard of care
    Other Names:
    • Radiation therapy
    • radiation oncology
  • Procedure: Align RT
    Standard of care
    Other Name: Image-Guided Radiation Therapy
Experimental: radiation therapy arm
Interventions:
  • Procedure: Radiotherapy
  • Procedure: Align RT
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
11
November 2011
March 2010   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients with HNC undergoing radiation therapy at Stanford University
  • Age >= 18 years old
  • Radiation course >= 4 weeks duration
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

  • Factors such as claustrophobia inhibiting use of thermoplastic mask immobilization device.
  • Patients who are pregnant or nursing, which preclude them from undergoing active radiation treatment.
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01011842
ENT0028
SU-09082009-3800 ( Other Identifier: Stanford University )
Yes
Not Provided
Not Provided
Quynh-Thu Le, Stanford University
Stanford University
Varian Medical Systems
Principal Investigator: Quynh-Thu Le Stanford University
Stanford University
May 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP
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