The purpose of this study is to test how the new 3D technology can be used to help improve the surgeon's ability to use information from standard imaging scans to guide head and neck surgery. Researchers will use the Scaniverse app during a standard ultrasound to create 3D images of participants' head and neck before their standard surgery. Researchers will see if the creation of a 3D framework profile with superimposed standard imaging scan information can be useful to the surgeon for guiding head and neck surgery
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
27
Preoperative imaging will be performed as part of the standard of care. Imaging data from US, CT, MRI, and/or PET performed for routine care will be used for this study.
3D images of surface landmarks will be acquired by use of US and the Scaniverse app before surgery, in conjunction with the participant's standard-of-care US or US-guided biopsy procedure
Memorial Sloan Kettering at Basking Ridge (Consent Only)
Basking Ridge, New Jersey, United States
RECRUITINGMemorial Sloan Kettering Monmouth (Consent only)
Middletown, New Jersey, United States
RECRUITINGMemorial Sloan Kettering Bergen (Consent only)
Montvale, New Jersey, United States
RECRUITINGMemorial Sloan Kettering Suffolk - Commack (Consent only)
Commack, New York, United States
RECRUITINGMemorial Sloan Kettering Westchester (Consent form)
Harrison, New York, United States
RECRUITINGMemorial Sloan Kettering Cancer Center (All protocol activites)
New York, New York, United States
RECRUITINGMemorial Sloan Kettering Nassau (Consent only)
Rockville Centre, New York, United States
RECRUITINGProportion of standard of care imaging studies successfully superimposed into 3D study framework for all participants
The primary objective of this study is to develop the technology of a 3D framework profile with superimposed preoperative imaging for intraoperative use. The process of developing the imaging technique will be considered successful if the imaging techniques and the hardware used are able to superimpose information from standard of care imaging studies into the 3D study framework for each participant.
Time frame: 1 year
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