A Study of the Use of 3D Technology to Guide Head and Neck Surgery

Memorial Sloan Kettering Cancer Center (MSK)

Status

Enrolling

Conditions

Surgery

Head and Neck Disorder

Treatments

Diagnostic Test: 3D framework

Diagnostic Test: Preoperative imaging

Study type

Interventional

Funder types

Other

Identifiers

NCT06676592

24-191

Details and patient eligibility

About

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

Enrollment

27 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Aged ≥18 years
Scheduled to undergo head and neck surgery in the Surgery Head and Neck Service at MSK

o Note: If, for some reason, the participant is not scheduled to have standard preoperative imaging procedures, then the participant will have an ultrasound of the head and neck for research purposes.
Scheduled to undergo standard of care preoperative imaging (ie, ultrasound (US), computed tomography (CT), magnetic resonance imaging (MRI), or positron emission tomography (PET)) in the Radiology Service at MSK
Ability to understand and sign (or their legally acceptable representative (LAR) must sign) the written informed consent

Exclusion criteria

Previous head and neck surgery or head and neck radiation
Any condition which, in the judgement of the clinical investigator or his designee, might increase the risk to the subject or decrease the chance of obtaining satisfactory data to achieve the objectives of the study