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Navigation Support With Mixed Reality With CORTEXPLORER MED (CXmed)

Primary Purpose

Cranial Aneurysm

Status
Completed
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
CORTEXPLORER MED
Sponsored by
cortEXplore GmbH
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Cranial Aneurysm focused on measuring Neuronavigation, Neurosurgery, Aneurysm, Surgical navigation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients of any gender in the age older or eqal 18 years
  • Patients who be informed of the nature of the clinical investigation and provide written informed consent
  • Patients with a cerebral aneurysm for which surgical clipping is indicated
  • Patients with a cerebral aneurysm where clipping is not routinely supported by navigation
  • Patients with current (not longer than 4 months) 3D image data of the brain

Exclusion Criteria:

  • Patients for whom required imaging is not available
  • Patients with ruptured cerebral aneurysm
  • Detained patients
  • Patients performing mandatory military service / community service
  • Patients who refuse to participate in the clinical investigation
  • Pregnant or nursing patients
  • Patients who are not able to sign the consent form
  • Patients who do not speak German
  • Patients who are taking part in any other clinical investigations

Sites / Locations

  • Kepler Universitätsklinikum

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

CORTEXPLORER MED

Arm Description

Mixed-reality assisted planning of aneurysm clipping with the optical navigation system CORTEXPLORER MED.

Outcomes

Primary Outcome Measures

Estimated trajectory with mixed-reality (without projection of trajectory)
Difference of angle and position of the estimated trajectory with mixed-reality support and without the projected trajectory compared to the pre-operatively defined trajectory.
Estimated trajectory without mixed-reality
Difference of angle and position of the estimated trajectory without mixed reality support (conventional) compared to the pre-operatively defined trajectory.

Secondary Outcome Measures

Estimated trajectory with mixed-reality (with projection of trajectory)
Difference of angle and position of the estimated trajectory with mixed reality support and with the projected trajectory compared to the pre-operatively defined trajectory.
Estimated trajectory with navigation support (planning view)
Difference of angle and position of the estimated trajectory with navigation support (planning view) compared to the pre-operatively defined trajectory.
Estimated trajectory with navigation support (navigation view)
Difference of angle and position of the estimated trajectory with navigation support (navigation view) and with the projected trajectory compared to the pre-operatively defined trajectory.
Planning performance with CORTEXPLORER MED
The distance to vessels and the distance from the cranial surface to the target of the post-surgical planning and the initial estimation of the trajectory (conventional approach).
Registration accuracy
The registration accuracy is measured with the navigation software in millimeters
Usability questionnaire
Usability questionnaire related to the activities preparation, planning, navigation and post-processing [0 - 5]
Degree of disability or limitation
Degree of disability or limitation in the daily activities of patients after neurological interventions as measured with the Modified Rankin Scale
Intraoperative complications
Severity and occurrence of seizures and bleedings and other intraoperative adverse events
Postoperative complications
Severity and occurrence of seizures and bleedings and other postoperative adverse events.

Full Information

First Posted
February 25, 2022
Last Updated
September 6, 2023
Sponsor
cortEXplore GmbH
Collaborators
Raffeiner GmbH
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1. Study Identification

Unique Protocol Identification Number
NCT05269498
Brief Title
Navigation Support With Mixed Reality With CORTEXPLORER MED
Acronym
CXmed
Official Title
Navigation Support With Mixed Reality for Surgical Clipping of Cerebral Aneurysms in Adult Patients With CORTEXPLORER MED - a Pilot Stage, Exploratory, First in Human Clinical Investigation
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
June 8, 2022 (Actual)
Primary Completion Date
June 1, 2023 (Actual)
Study Completion Date
June 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
cortEXplore GmbH
Collaborators
Raffeiner GmbH

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
During the last 15 years, neuronavigation has become an essential neurosurgical tool for pursuing minimal invasiveness and safety. One drawback of such devices is the fact, that the neurosurgeon has to look away from the surgical field onto a dedicated workstation screen. Additionally, the operator is required to transfer this information from the "virtual" environment of the navigation system to the real surgical field - whereas the real patient may be fixated and positioned differently compared to the visualization on the screen. Mixed-reality may have the potential to support this, by merging data from the real environment with virtual information and vice-versa. In the context of surgical navigation, the main goal of mixed reality systems is to provide a real-time updated 3D virtual model of anatomical details, overlaid on the real surgical field. In this sense, the mixed reality is the process of enrichment of reality with additional virtual contents. This clinical investigation aims at the collecting of clinical data about the mixed-reality supported planning, the registration accuracy and overall precision of the navigation system and the clinical outcome.
Detailed Description
The CORTEXPLORER MED system is a platform that enables surgical navigation using radiological images of patients. The application software reads, formats and merges patient-specific multimodal images such as pre-surgical computed tomography (CT), magnetic resonance imaging (MRI, fMRI) as well as intraoperatively taken fluoroscopic scans. These digital representations of the patient are displayed on a computer screen from different anatomical perspectives (axial, sagittal, coronal, diagonal). Moreover, a 3D digital model can be computed based on the 2D imaging data. Before the operation, the surgeon can create, save, and simulate the course along one or more surgical trajectories. During surgery, the system tracks the position of specific surgical instruments in or on the patient's anatomy and continuously updates their position, which can be displayed on a computer screen or trough mixed reality glasses (Microsoft HoloLens). Generally, this clinical investigation aims at the collecting of clinical data to indicate the difference between the planning of a neurosurgery without and with the mixed reality feature of CORTEXPLORER MED. Additionally, clinical data is collected to indicate the difference between the planning of a surgery with the CORTEXPLORER MED and without the system (conventional approach for this indication). The data from this pilot phase are used for the planning of a larger clinical investigation and for the overall clinical evaluation of the navigation system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cranial Aneurysm
Keywords
Neuronavigation, Neurosurgery, Aneurysm, Surgical navigation

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CORTEXPLORER MED
Arm Type
Experimental
Arm Description
Mixed-reality assisted planning of aneurysm clipping with the optical navigation system CORTEXPLORER MED.
Intervention Type
Device
Intervention Name(s)
CORTEXPLORER MED
Intervention Description
The CORTEXPLORER MED system is a platform that enables surgical navigation using real-time radiological images of patients. The application software formats patient-specific computed tomography or magnetic resonance images taken before surgery. These are displayed on the screen and through mixed reality from different perspectives (axial, sagittal, coronal, diagonal). Before surgery, the surgeon can then create, save and simulate the course along one or more surgical trajectories. As a visualization aid, the surgeon can also create and edit one or more 3D models of the anatomy. During surgery, the system tracks the position of specific surgical instruments in or on the patient's anatomy and continuously updates the position of the instruments on these images.
Primary Outcome Measure Information:
Title
Estimated trajectory with mixed-reality (without projection of trajectory)
Description
Difference of angle and position of the estimated trajectory with mixed-reality support and without the projected trajectory compared to the pre-operatively defined trajectory.
Time Frame
Day 0
Title
Estimated trajectory without mixed-reality
Description
Difference of angle and position of the estimated trajectory without mixed reality support (conventional) compared to the pre-operatively defined trajectory.
Time Frame
Day 0
Secondary Outcome Measure Information:
Title
Estimated trajectory with mixed-reality (with projection of trajectory)
Description
Difference of angle and position of the estimated trajectory with mixed reality support and with the projected trajectory compared to the pre-operatively defined trajectory.
Time Frame
Day 0
Title
Estimated trajectory with navigation support (planning view)
Description
Difference of angle and position of the estimated trajectory with navigation support (planning view) compared to the pre-operatively defined trajectory.
Time Frame
Day 0
Title
Estimated trajectory with navigation support (navigation view)
Description
Difference of angle and position of the estimated trajectory with navigation support (navigation view) and with the projected trajectory compared to the pre-operatively defined trajectory.
Time Frame
Day 0
Title
Planning performance with CORTEXPLORER MED
Description
The distance to vessels and the distance from the cranial surface to the target of the post-surgical planning and the initial estimation of the trajectory (conventional approach).
Time Frame
Day 0, Day 30
Title
Registration accuracy
Description
The registration accuracy is measured with the navigation software in millimeters
Time Frame
Day 0
Title
Usability questionnaire
Description
Usability questionnaire related to the activities preparation, planning, navigation and post-processing [0 - 5]
Time Frame
Day 0, Day 30
Title
Degree of disability or limitation
Description
Degree of disability or limitation in the daily activities of patients after neurological interventions as measured with the Modified Rankin Scale
Time Frame
Day 7
Title
Intraoperative complications
Description
Severity and occurrence of seizures and bleedings and other intraoperative adverse events
Time Frame
Day 0
Title
Postoperative complications
Description
Severity and occurrence of seizures and bleedings and other postoperative adverse events.
Time Frame
Day 1 to Day 7

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients of any gender in the age older or eqal 18 years Patients who be informed of the nature of the clinical investigation and provide written informed consent Patients with a cerebral aneurysm for which surgical clipping is indicated Patients with a cerebral aneurysm where clipping is not routinely supported by navigation Patients with current (not longer than 4 months) 3D image data of the brain Exclusion Criteria: Patients for whom required imaging is not available Patients with ruptured cerebral aneurysm Detained patients Patients performing mandatory military service / community service Patients who refuse to participate in the clinical investigation Pregnant or nursing patients Patients who are not able to sign the consent form Patients who do not speak German Patients who are taking part in any other clinical investigations
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthias Gmeiner, MD
Organizational Affiliation
Johannes-Kepler-University, Department of Neurosurgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kepler Universitätsklinikum
City
Linz
State/Province
Upper Austria
ZIP/Postal Code
4020
Country
Austria

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://www.cortexplore.com
Description
Homepage of manufacturer

Learn more about this trial

Navigation Support With Mixed Reality With CORTEXPLORER MED

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