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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

11 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-10-31

Study Completion Date

2011-11-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Head and Neck Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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radiation therapy arm

Group Type EXPERIMENTAL

Radiotherapy

Intervention Type PROCEDURE

Standard of care

Align RT

Intervention Type PROCEDURE

Standard of care

Interventions

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Radiotherapy

Standard of care

Intervention Type PROCEDURE

Align RT

Standard of care

Intervention Type PROCEDURE

Other Intervention Names

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Radiation therapy radiation oncology Image-Guided Radiation Therapy

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No