A Study of the Use of 3D Technology to Guide Head and Neck Surgery
NCT ID: NCT06676592
Last Updated: 2025-10-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
27 participants
INTERVENTIONAL
2024-11-01
2027-11-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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Participants scheduled for head and neck surgery
Participants are scheduled to undergo head and neck surgery in the Surgery Head and Neck Service at MSK
Preoperative imaging
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 framework
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
Interventions
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Preoperative imaging
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 framework
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
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
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Memorial Sloan Kettering Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Snehal Patel, MD
Role: PRINCIPAL_INVESTIGATOR
Memorial Sloan Kettering Cancer Center
Locations
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Memorial Sloan Kettering at Basking Ridge (Consent Only)
Basking Ridge, New Jersey, United States
Memorial Sloan Kettering Monmouth (Consent only)
Middletown, New Jersey, United States
Memorial Sloan Kettering Bergen (Consent only)
Montvale, New Jersey, United States
Memorial Sloan Kettering Suffolk - Commack (Consent only)
Commack, New York, United States
Memorial Sloan Kettering Westchester (Consent form)
Harrison, New York, United States
Memorial Sloan Kettering Cancer Center (All protocol activites)
New York, New York, United States
Memorial Sloan Kettering Nassau (Consent only)
Rockville Centre, New York, United States
Countries
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Central Contacts
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Facility Contacts
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Snehal Patel, MD
Role: primary
Snehal Patel, MD
Role: primary
Snehal Patel, MD
Role: primary
Snehal Patel, MD
Role: primary
Snehal Patel, MD
Role: primary
Snehal Patel, MD
Role: primary
Snehal Patel, MD
Role: primary
Related Links
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Memorial Sloan Kettering Cancer Center
Other Identifiers
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24-191
Identifier Type: -
Identifier Source: org_study_id
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