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Non-contact Intraoperative Optical Imaging During Neurosurgical Procedures

Non-contact Intraoperative Optical Imaging During Neurosurgical Procedures

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03391011
Enrollment
40
Registered
2018-01-05
Start date
2015-03-13
Completion date
2019-03-13
Last updated
2018-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Computer-assisted Surgery

Brief summary

For a significant number of patients suffering from back pain, even basic daily activities become impossible. It is at this time that spinal surgery becomes necessary in order to improve the patient's quality of life. To combat these symptoms, surgical implants (e.g. pedicle screws, rods, etc.) are used to aid in stabilizing and correcting the deformities of the spine, particularly after spinal decompression. The clinical need for spinal surgery is compounded by current and continuing demographic trends. As the general population continues to age, the number of orthopaedic surgical interventions is expected to rise drastically. Therefore, a significant opportunity exists for the implementation of surgical guidance technologies, for orthopaedic procedures, to combat this overwhelming health care burden.

Detailed description

The hypothesis is that optical visualization of surgically exposed anatomy with the Biophotonics and Bioengineering Lab (BBL) surgical navigation prototype, when registered with pre-operative imaging (CT or MRI), can accurately estimate subsurface anatomy and allow tracking the position of surgical instruments in real-time, using an intraoperative non-contact optical imaging system during spinal surgical procedures.

Interventions

Comparison of accuracy of screw placement using experimental system while monitored by clinically approved system.

Sponsors

Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Greater than 18 years of age, able to provide consent, or has substitute decision maker available to consent. * Scheduled to undergo spinal instrumentation surgery involving pedicle or lateral mass screw insertion. * Scheduled for pre-operative CT scan and the surgical plan includes open exposure of the posterior bony elements of two or more level(s) of the vertebra(e). * No contra-indication for a post-operative CT scan.

Exclusion criteria

* Previous spinal decompression with significant laminectomy performed at the level intended for instrumentation. * Previous spinal instrumentation with significant metallic artefact on pre-operative CT scan

Design outcomes

Primary

MeasureTime frameDescription
Pilot hole and screw trajectory accuracy as compared between post-operative CT and intraoperative imagesWithin 1 week of screw placementComparison and quantification of accuracy of pilot holes including entry point and trajectory as taken from experimental navigation system as compared to absolute (or actual) entry point and trajectory of screws as determined by post-operative computed tomography scans.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026