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Study identifier: NCT06676592 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

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

Condition: Surgery · Head and Neck Disorder  ·  Sponsor: Memorial Sloan Kettering Cancer Center

PhaseNA
Planned participants27
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where7 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

Snehal Patel, MD  ·  212-639-3412  ·  patels@mskcc.org

Joseph Stember, MD  ·  StemberJ@mskcc.org

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

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

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (7)

Memorial Sloan Kettering at Basking Ridge (Consent Only)Basking Ridge, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Monmouth (Consent only)Middletown, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Bergen (Consent only)Montvale, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Suffolk - Commack (Consent only)Commack, New York, United StatesRecruiting
Memorial Sloan Kettering Westchester (Consent form)Harrison, New York, United StatesRecruiting
Memorial Sloan Kettering Cancer Center (All protocol activites)New York, New York, United StatesRecruiting
Memorial Sloan Kettering Nassau (Consent only)Rockville Centre, New York, United StatesRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

Basking RidgeMiddletownMontvaleCommack

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