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The Performance of a Robot-assisted Minimally Invasive Direct Cochlear Access for Cochlear Implantation

Primary Purpose

Sensorineural Hearing Loss

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
HEARO
OTOPLAN
Sponsored by
Insel Gruppe AG, University Hospital Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sensorineural Hearing Loss

Eligibility Criteria

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

Inclusion Criteria:

  • Subjects scheduled for CI surgery according to clinical routine
  • Subjects who will receive a cochlear implant
  • Signed and dated informed consent form

Exclusion Criteria:

  • Lack of compliance with any inclusion criteria
  • Age under 18 years
  • Pregnancy
  • Distance of the planned trajectory to the facial nerve is < 0.4 mm as per screening CT scan
  • Distance of the planned trajectory to the chorda tympani is < 0.3 mm as per screening CT scan
  • A safe inner ear access cannot be planned for preservation of RW membrane and cochlear structures
  • Individuals where image guidance or robotic procedures are not indicated

Sites / Locations

  • Inselspital, Bern University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

RCI-BE-10

Arm Description

Robot assisted cochlear implant surgery.

Outcomes

Primary Outcome Measures

Relative ratio of successful electrode array insertions through the drilled direct cochlear access with the HEARO procedure to the total HEARO procedures.
The primary outcome measure of this study is to explore the relative ratio of the successful electrode array insertions into the cochlea through the drilled direct cochlear access with the HEARO procedure to the total HEARO procedures. Aborted or converted procedures count as procedure in which insertion through the direct cochlea access was not possible. The results will be expressed in relative numbers and in percentage.

Secondary Outcome Measures

Electrode array insertion outcome
The angular insertion depth (in degrees) will be evaluated.
Electrode array insertion outcome
The number of inserted electrode contacts will be evaluated.
Electrode array insertion outcome
The surgical outcome (categories: nominal, tip-fold over or scalar deviation) will be evaluated.
Insertion depth prediction accuracy
The insertion depth prediction accuracy as the difference between the estimated insertion depth of the electrode at the planning and the actual insertion depth.
Absolute angular accuracy of the drilled tunnel access
The absolute in-plane and out-plane accuracy of the drilled tunnel is measured as the angular deviation between the planned trajectory in-plane and out-plane angles and the actual drilled angles from the intra-op image.
Absolute lateral accuracy of the drilled tunnel at the facial recess
The absolute lateral accuracy of the drilled tunnel to the facial nerve and chorda tympani is measured as the difference between the planned trajectory and the actual drilled trajectory distance.
Absolute lateral accuracy of the drilled tunnel at the target
The absolute lateral accuracy of the drilled tunnel is measured as the distance between the planned target trajectory position and actual target of the drilled trajectory position.
Ratio of the round window membrane preservation during the inner ear access
The ratio of the visibility of round window membrane surface at the robotic inner ear access by visual inspection. This will be assessed as subjective evaluation by the surgeon.
Timing of the HEARO procedure
The timing of the different steps of the HEARO procedure will be recorded.

Full Information

First Posted
October 22, 2020
Last Updated
November 23, 2022
Sponsor
Insel Gruppe AG, University Hospital Bern
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1. Study Identification

Unique Protocol Identification Number
NCT04610450
Brief Title
The Performance of a Robot-assisted Minimally Invasive Direct Cochlear Access for Cochlear Implantation
Official Title
The Performance of a Robot-assisted Minimally Invasive Direct Cochlear Access for Cochlear Implantation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
April 26, 2021 (Actual)
Primary Completion Date
November 23, 2022 (Actual)
Study Completion Date
November 23, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern

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
The cochlear implant is a neural prosthesis and has been the gold standard treatment for severe to profound sensorineural hearing loss over several decades. The surgical procedure for cochlear implantation aims to atraumatically insert the electrode array of the cochlear implant into the cochlea. However, due to the location of the cochlea inside the skull, the surgeon is required to create an access from the surface of the temporal bone to the cochlea (inner ear). In conventional methods, this access is acquired by removal of portions of the mastoid bone through a mastoidectomy and posterior tympanotomy. The outcome and success of the conventional procedure varies due to mainly two factors: surgeon skill and subject anatomical variation. To overcome these variables toward a more consistent and less invasive cochlear implantation surgery, the development of robotic and image guided cochlear implantation has taken place. This study primarily aims to explore the performance of robotic cochlear implantation surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sensorineural Hearing Loss

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
RCI-BE-10
Arm Type
Experimental
Arm Description
Robot assisted cochlear implant surgery.
Intervention Type
Device
Intervention Name(s)
HEARO
Intervention Description
Robotic system for otological procedures
Intervention Type
Device
Intervention Name(s)
OTOPLAN
Intervention Description
Otological surgical planning software
Primary Outcome Measure Information:
Title
Relative ratio of successful electrode array insertions through the drilled direct cochlear access with the HEARO procedure to the total HEARO procedures.
Description
The primary outcome measure of this study is to explore the relative ratio of the successful electrode array insertions into the cochlea through the drilled direct cochlear access with the HEARO procedure to the total HEARO procedures. Aborted or converted procedures count as procedure in which insertion through the direct cochlea access was not possible. The results will be expressed in relative numbers and in percentage.
Time Frame
day 0
Secondary Outcome Measure Information:
Title
Electrode array insertion outcome
Description
The angular insertion depth (in degrees) will be evaluated.
Time Frame
day 0
Title
Electrode array insertion outcome
Description
The number of inserted electrode contacts will be evaluated.
Time Frame
day 0
Title
Electrode array insertion outcome
Description
The surgical outcome (categories: nominal, tip-fold over or scalar deviation) will be evaluated.
Time Frame
day 0
Title
Insertion depth prediction accuracy
Description
The insertion depth prediction accuracy as the difference between the estimated insertion depth of the electrode at the planning and the actual insertion depth.
Time Frame
day 0
Title
Absolute angular accuracy of the drilled tunnel access
Description
The absolute in-plane and out-plane accuracy of the drilled tunnel is measured as the angular deviation between the planned trajectory in-plane and out-plane angles and the actual drilled angles from the intra-op image.
Time Frame
day 0
Title
Absolute lateral accuracy of the drilled tunnel at the facial recess
Description
The absolute lateral accuracy of the drilled tunnel to the facial nerve and chorda tympani is measured as the difference between the planned trajectory and the actual drilled trajectory distance.
Time Frame
day 0
Title
Absolute lateral accuracy of the drilled tunnel at the target
Description
The absolute lateral accuracy of the drilled tunnel is measured as the distance between the planned target trajectory position and actual target of the drilled trajectory position.
Time Frame
day 0
Title
Ratio of the round window membrane preservation during the inner ear access
Description
The ratio of the visibility of round window membrane surface at the robotic inner ear access by visual inspection. This will be assessed as subjective evaluation by the surgeon.
Time Frame
day 0
Title
Timing of the HEARO procedure
Description
The timing of the different steps of the HEARO procedure will be recorded.
Time Frame
day 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects scheduled for CI surgery according to clinical routine Subjects who will receive a cochlear implant Signed and dated informed consent form Exclusion Criteria: Lack of compliance with any inclusion criteria Age under 18 years Pregnancy Distance of the planned trajectory to the facial nerve is < 0.4 mm as per screening CT scan Distance of the planned trajectory to the chorda tympani is < 0.3 mm as per screening CT scan A safe inner ear access cannot be planned for preservation of RW membrane and cochlear structures Individuals where image guidance or robotic procedures are not indicated
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marco Caversaccio, Prof. Dr.
Organizational Affiliation
University Hospital Bern (Inselspital)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Inselspital, Bern University Hospital
City
Bern
ZIP/Postal Code
3010
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Performance of a Robot-assisted Minimally Invasive Direct Cochlear Access for Cochlear Implantation

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