Spine Registration Using 3D Scanning

Sponsor
Advanced Scanners Inc. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05195580
Collaborator
(none)
10
1
12
0.8

Study Details

Study Description

Brief Summary

The primary objective is to assess the capability of the device as measured by its consistency, its accuracy, and feedback from surgical staff over the study period.

Condition or Disease Intervention/Treatment Phase
  • Device: Optical 3D Scanner

Study Design

Study Type:
Observational
Anticipated Enrollment :
10 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Pre-pilot Study of Spine Registration Using 3D Scanning
Actual Study Start Date :
Aug 31, 2021
Anticipated Primary Completion Date :
Aug 31, 2022
Anticipated Study Completion Date :
Aug 31, 2022

Outcome Measures

Primary Outcome Measures

  1. Spine Registration [Throughout the surgical procedure]

    Closely match the Advanced Scanners optical scan of the partially exposed surface of the patient vertebra to the corresponding patient's preoperative MRI and/or CT scan, thereby learning the position of the rest of the vertebra. This endpoint includes registration of the relevant preoperative MRI or CT scan portion to the portion scanned by Advanced Scanners.

Secondary Outcome Measures

  1. Vertebral Shift Measurement [Throughout the surgical procedure]

    Use the intraoperative x-ray (typically O-arm) measurements taken at various times in the procedure to validate the capability of our scanner to determine relative shifts between vertebra as a function of time.

  2. Determination Of Bony Exposure Requirements [Throughout the surgical procedure]

    Measure the area of the exposed vertebra of registered adjacent segments. Bone regions will be identified in the scan mesh, segmented from the rest of the scan, and their areas determined directly from that surface region by integrating the area of the relevant mesh faces, in units of square millimeters or square centimeters.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Patients that require exposure of bony posterior spine anatomy for localization as standard of care.

  2. Clinically planned for spine surgery.

  3. Able to provide written informed consent from subject or subject's legal representative, using IRB approved consent form, and ability for subject to comply with the protocol requirements of the study.

Exclusion Criteria:
  1. Language problems that would prevent from properly understanding instructions.

  2. Requirement of an interpreter.

  3. Patients who are excluded from consideration for the surgical procedure are therefore excluded from the research study.

  4. Special populations: pregnant women, prisoners.

  5. Minimally invasive spine surgery that does not expose the necessary bone/s.

  6. Spine surgery without posterior exposure.

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. David's Round Rock Medical Center Round Rock Texas United States 78681

Sponsors and Collaborators

  • Advanced Scanners Inc.

Investigators

  • Study Director: Aaron Bernstein, PhD, Advanced Scanners Inc.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Advanced Scanners Inc.
ClinicalTrials.gov Identifier:
NCT05195580
Other Study ID Numbers:
  • 01500
First Posted:
Jan 19, 2022
Last Update Posted:
Jan 19, 2022
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 19, 2022