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.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorImperial College London

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial population

Adult spine surgery candidates treated within the Imperial College Healthcare NHS Trust , with the capacity to consent (non-vulnerable)

Trial design

Design model

Other

Time perspective

Retrospective

Treatments tested in this trial

  • Spine surgery

    Procedure/Surgery

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

Treatment groups

25 Participants
are divided into 1 treatment group
Group A: Spine Surgery Patients1 intervention

Trial outcomes

Primary outcomes

1

Number of Data Collection completed

Success in recording 25 RGB-D videos of spine surgeries along with corresponding CT scans

Time frame
3 years (initial recording duration)
2

Number of Data points collected containing a variety of exposed spine anatomy

Collected samples should contain a wide variety of exposed vertebrae, including cervical, thoracic and lumbar vertebrae

Time frame
3 years (initial recording duration)
3

Patient diversity in Ethnicity

Patients undergoing surgery should be diverse in terms of ethnicity, diversity being the % of patients who are not 'white british'

Time frame
3 years (initial recording duration)
4

Patient diversity in Age

Patients undergoing surgery should be diverse in terms of age, diversity being captured by range and standard deviation measures

Time frame
3 years (initial recording duration)

Secondary outcomes

1

Usefulness for training navigation system

Outcome is to leverage the recordings to train a markerless tracking system that will intraoperatively track the pose and location of the spine within the surgical site. The trained system will be benchmarked against a test subset of the collected videos. The success of the trained system will be determined by its accuracy in automatically tracking the pose of vertebrae features within the test subset videos, against the labelled pose indicated in the video by the operating surgeon.

Time frame
4 years (initial recording duration + 1)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Imperial College London

Lead sponsor

Imperial College Healthcare NHS Trust

Collaborator

This trial is not recruiting at the moment. You can still explore other options: