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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.

NCT ID: NCT06580379

Last Updated: 2024-08-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

25 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-10-31

Study Completion Date

2027-10-31

Brief Summary

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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.

Detailed Description

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Conditions

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Spine Fusion Spine Injury Spine Degeneration Navigation, Spatial

Keywords

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Imaging Depth Imaging Spine Surgery Intraoperative Registration

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

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Spine Surgery Patients

non-vulnerable adults undergoing spine surgery, with a posterior approach

Spine surgery

Intervention Type PROCEDURE

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

Interventions

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Spine surgery

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

Intervention Type PROCEDURE

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Imperial College Healthcare NHS Trust

OTHER

Sponsor Role collaborator

Imperial College London

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Salvatore Russo, MD

Role: PRINCIPAL_INVESTIGATOR

Imperial College Healthcare Trust

Central Contacts

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Connor Daly, MEng

Role: CONTACT

Phone: 7528869070

Email: [email protected]

Other Identifiers

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168041

Identifier Type: -

Identifier Source: org_study_id