The investigators propose here to evaluate the feasibility of a novel cone-beam CT (CBCT)-guided online adaptive radiotherapy (ART) workflow on the Halcyon device.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Enrollment
37
Each imaging session will be less than one hour, and is expected to take no more than 15 minutes.
Washington University School of Medicine
St Louis, Missouri, United States
Feasibility of the device as measured by successful completion of the full CBCT-guided online ART workflow, from volumetric imaging through phantom delivery in at least 90% of attempted fractions
Time frame: Completion of ART workflow in all enrolled participants (estimated to be 30 months)
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