MedPath

Augmented Reality Enhanced Surgery: Use of Holographic Technology in Cranial and Spinal Surgery

Completed
Conditions
Surgery
Interventions
Device: Augmented Reality Headset
Registration Number
NCT03921385
Lead Sponsor
University of Pennsylvania
Brief Summary

* To demonstrate the feasibility of integrating holographic technology as a heads-up display for navigated cranial and spinal neurosurgical procedures. This entails simply displaying the navigation screen currently used by Medtronic Stealth or Brainlab systems as a holographic image that can be positioned closer to the operative field.

* To develop a systematic, efficient communication and registration process allowing holographic technology to be potentially utilized as a navigation tool in cranial and spinal neurosurgery. This entails developing software, optimizing connection parameters, and devising registration techniques incorporating line-of-sight fiducial markers to allow the holographic device to function as a navigation instrument.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • age >= 18
  • must be able to read and understand English, and sign the informed consent form
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Exclusion Criteria
  • emergent/emergency procedures
  • pediatric patients
  • pregnant patients
  • vulnerable populations
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Single cohort - navigated cranial and spine surgeryAugmented Reality Headset-
Primary Outcome Measures
NameTimeMethod
Assessment of holographic technology in the operating room using a feasibility scale ranging from 1-102 years

To demonstrate the feasibility of integrating holographic technology as a heads-up display for navigated cranial and spinal neurosurgical procedures. This entails simply displaying the navigation screen currently used by Medtronic Stealth or Brainlab systems as a holographic image that can be positioned closer to the operative field.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Pennsylvania Medical Center

🇺🇸

Philadelphia, Pennsylvania, United States

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