Clinical trial · Interventional
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
NCT01011842CI-TRIAL-00038023terminatedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Head and Neck Cancer | Malignant Head and Neck Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Align RT | Procedure | — | UNRESOLVED |
| Radiotherapy | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- radiation therapy arm
- interventionNames
- Procedure: Radiotherapy
- Procedure: Align RT
Primary outcomes (1)
- measure
- We are measuring how much a patient moves during treatment.
- timeFrame
- This information will be available immediately have the patient is treated.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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.
References
Publications (0)
Data not yet available
No reference posted for this study.