NCT06676592

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

Digitally Acquired 3D Framework With Superimposed Preoperative Imaging Data for Intraoperative Guidance

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 27 (estimated)
• Sponsor: Memorial Sloan Kettering Cancer Center · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

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

Conditions

• Surgery
• Head and Neck Disorder

Interventions

Type	Name	Description
DIAGNOSTIC_TEST	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.
DIAGNOSTIC_TEST	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

Timeline

• Start date: 2024-11-01
• Primary completion: 2027-11-01
• Completion: 2027-11-01
• First posted: 2024-11-06
• Last updated: 2025-10-09

Locations

7 sites across 1 country: United States