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Not yet recruiting NCT06580379

Spine Surgery Video Observation Study. The Creation of a Benchmark Video (RGB-Depth) Dataset to Investigate the Feasibility of Developing a Markerless Tracking System for Spine Surgery.

Observational Spine Fusion Spine Injury Spine Degeneration Navigation, Spatial

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Spine surgery.
Who it may be relevant to
Registry conditions: Spine Fusion, Spine Injury, Spine Degeneration, Navigation, Spatial. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The primary study objective is to build a video dataset, consisting of both colour and depth information, of spine surgery that includes both 'open' and 'minimally invasive' (MIS) surgeries. Using accompanying preoperative CT scans of the patient's spine, we aim to develop a markerless tracking system for spine surgery, which the collected dataset will be used to both train, and then benchmark against.

Interventions

  • Procedure Spine surgery
    Spine surgery, such as fusion requiring the need for precise intraoperative registration and navigation

Primary outcome measures

  • Number of Data Collection completed [Time frame: 3 years (initial recording duration)]
  • Number of Data points collected containing a variety of exposed spine anatomy [Time frame: 3 years (initial recording duration)]
  • Patient diversity in Ethnicity [Time frame: 3 years (initial recording duration)]
  • Patient diversity in Age [Time frame: 3 years (initial recording duration)]
Secondary outcome measures (1)
  • Usefulness for training navigation system [Time frame: 4 years (initial recording duration + 1)]

Eligibility criteria

Inclusion criteria

  • Candidate surgeries include all spine surgeries taking a posterior approach. This includes both 'open' and 'minimally invasive' surgeries, provided some portion of vertebrae bone is exposed.

Exclusion criteria

  • Candidate surgeries will be excluded if the patient is under the age of 18 or the clinical lead feels the patient lacks capacity to consent.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06580379 · 168041

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗