Long Term Results With the Vibrant Soundbridge in Patients With Mixed Hearing Loss: a 60-month Longitudinal Study

Sponsor
MED-EL Elektromedizinische Geräte GesmbH (Industry)
Overall Status
Completed
CT.gov ID
NCT05793580
Collaborator
(none)
31
1
1
120
0.3

Study Details

Study Description

Brief Summary

Vibrant Soundbridge (VSB, MED-EL, Innsbruck) Active middle ear implants (AMEI) can benefit patients who are unable to use conventional hearing aids (HA) due to medical reasons, discomfort or unsuccessful rehabilitation. Long-term prospective longitudinal studies are lacking on the VSB notably for conductive and mixed hearing loss. The main aim of the present study was to prospectively assess aided hearing benefits in a 60-month, long-term study including conductive and mixed hearing loss adults implanted with the VSB. The secondary objective was to compare the hearing results according to the Floating Mass Transducer (FMT) site (Round/oval window (RW/OW) vs incus/stapes) and the type of pathology responsible for the hearing loss (Inflammatory vs non-inflammatory disease, ID vs NID).

Condition or Disease Intervention/Treatment Phase
  • Device: Vibrant Soundbridge active middle ear implant
N/A

Detailed Description

Introduction:

Active middle ear implants (AMEI) can benefit patients who are unable to use conventional hearing aids (HA) due to medical reasons, discomfort or unsuccessful rehabilitation.

AMEIs provide more hearing gain and consistency compared to middle ear surgery plus conventional hearing aids. Coletti et al. (2013) reported on long-term outcomes of patients implanted at the round window (RW) with the VSB. Brkic et al. (2019) presented a large number of subjects (n = 23) with a 20-year follow-up. The limitations of these studies were their retrospective design.

The best location for the surgeon to place the VSB's floating mass transducer (FMT) depends on various factors. A meta-analysis showed the hearing results at different FMT sites to be similar. None of these studies compared a FMT placed to a FMT clipped.

The impact of the etiology of deafness on a patient's outcome with an AMEI has been poorly studied. Only one study has shown that the difference between inflammatory disease (ID) and non-inflammatory disease (NID) groups was not significant.

The main objective:

Prospectively assess aided hearing benefits in a 60-month, long-term study including conductive and mixed hearing loss adults implanted with the VSB.

Measures are tonal audiometry, pure-tone average (PTA), vocal audiometry in quiet, 50% speech recognition threshold (SRT) in quiet, word recognition in quiet (WRS) at 65 dB sound pressure level (SPL), word recognition in noise (WRSN ; speech at 65 dB SPL and 0°, white noise at 55 dB SPL and 180°. signal-to-noise ratio = 10 dB).

The secondary objectives:

Comparison of the hearing results according to the FMT site (RW/OW to incus/stapes)

Comparison of the hearing results according the type of pathology responsible for the hearing loss (ID to NID).

Plan of the study:

It is a multicentric, prospective, longitudinal study with 6 tertiary references centres with a follow up over a period of 60 months.

Measures will be done on the patient preoperatively and 1, 3, 6, 12 and 60 months post-implantation.

Preoperative measures will be done also with hearing aid (HA) and bone-anchored hearing aid on a headband (HBAHA).

Study Design

Study Type:
Interventional
Actual Enrollment :
31 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Prospective longitudinal studyProspective longitudinal study
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Long Term Results With the Vibrant Soundbridge in Patients With Mixed Hearing Loss: a Prospective Multicenter Longitudinal Study Over 60-months
Actual Study Start Date :
Sep 1, 2008
Actual Primary Completion Date :
Sep 1, 2018
Actual Study Completion Date :
Sep 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Other: VSB arm

longitudinal follow-up of VSB users preoperatively and at 1, 3, 6, 12 and 60 months post-implantation.

Device: Vibrant Soundbridge active middle ear implant
active middle ear implant

Outcome Measures

Primary Outcome Measures

  1. Tonal audiometry [preoperatively]

    Pure-tone audiograms

  2. Tonal audiometry [at 1 month post-implantation]

    Pure-tone audiograms

  3. Tonal audiometry [at 3 months post-implantation]

    Pure-tone audiograms

  4. Tonal audiometry [at 6 months post-implantation]

    Pure-tone audiograms

  5. Tonal audiometry [at 12 months post-implantation]

    Pure-tone audiograms

  6. Tonal audiometry [at 60 months post-implantation]

    Pure-tone audiograms

Secondary Outcome Measures

  1. Word recognition in quiet [preoperatively]

    Speech recognition test of disyllabic words (Fournier lists).

  2. Word recognition in quiet [at 1 month post-implantation]

    Speech recognition test of disyllabic words (Fournier lists).

  3. Word recognition in quiet [at 3 months post-implantation]

    Speech recognition test of disyllabic words (Fournier lists).

  4. Word recognition in quiet [at 6 months post-implantation]

    Speech recognition test of disyllabic words (Fournier lists).

  5. Word recognition in quiet [at 12 months post-implantation]

    Speech recognition test of disyllabic words (Fournier lists).

  6. Word recognition in quiet [at 60 months post-implantation]

    Speech recognition test of disyllabic words (Fournier lists).

  7. Word recognition in noise [preoperatively]

    Speech recognition test of disyllabic words (Fournier lists) in noise. Noise = white noise at 55 dB SPL presented at 180°. Speech at 65 dB SPL presented at 0°.

  8. Word recognition in noise [at 1 month post-implantation]

    Speech recognition test of disyllabic words (Fournier lists) in noise. Noise = white noise at 55 dB SPL presented at 180°. Speech at 65 dB SPL presented at 0°.

  9. Word recognition in noise [at 3 months post-implantation]

    Speech recognition test of disyllabic words (Fournier lists) in noise. Noise = white noise at 55 dB SPL presented at 180°. Speech at 65 dB SPL presented at 0°.

  10. Word recognition in noise [at 6 months post-implantation]

    Speech recognition test of disyllabic words (Fournier lists) in noise. Noise = white noise at 55 dB SPL presented at 180°. Speech at 65 dB SPL presented at 0°.

  11. Word recognition in noise [at 12 months post-implantation]

    Speech recognition test of disyllabic words (Fournier lists) in noise. Noise = white noise at 55 dB SPL presented at 180°. Speech at 65 dB SPL presented at 0°.

  12. Word recognition in noise [at 60 months post-implantation]

    Speech recognition test of disyllabic words (Fournier lists) in noise. Noise = white noise at 55 dB SPL presented at 180°. Speech at 65 dB SPL presented at 0°.

  13. Speech reception threshold [preoperatively]

    Speech reception threshold to have 50% of intelligibility on disyllabic words.

  14. Speech reception threshold [at 1 month post-implantation]

    Speech reception threshold to have 50% of intelligibility on disyllabic words.

  15. Speech reception threshold [at 3 months post-implantation]

    Speech reception threshold to have 50% of intelligibility on disyllabic words.

  16. Speech reception threshold [at 6 months post-implantation]

    Speech reception threshold to have 50% of intelligibility on disyllabic words.

  17. Speech reception threshold [at 12 months post-implantation]

    Speech reception threshold to have 50% of intelligibility on disyllabic words.

  18. Speech reception threshold [at 60 months post-implantation]

    Speech reception threshold to have 50% of intelligibility on disyllabic words.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult patient (>= 18 years old) speaking French

  • with mixed hearing loss on at least one side

  • with a maximum bone conduction (BC) threshold of 45 dB hearing level (HL) at 500 Hz, 50 dB HL at 1000 Hz, 55 dB HL at 1500 Hz, and 60 dB HL at 2000 Hz.

  • with a 20 dB minimum air-bone gap (defined as the difference between bone- and air conduction thresholds).

  • with stable BC thresholds over the previous 24 months, and no sufficient benefit with the HA.

Exclusion Criteria:
  • fluctuating hearing loss,

  • cutaneous disease

  • subjects who need an MRI.

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Rennes Rennes France 35000

Sponsors and Collaborators

  • MED-EL Elektromedizinische Geräte GesmbH

Investigators

  • Principal Investigator: Benoît Godey, Pr, Rennes University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
MED-EL Elektromedizinische Geräte GesmbH
ClinicalTrials.gov Identifier:
NCT05793580
Other Study ID Numbers:
  • VSB_longterm_Rennes_study
First Posted:
Mar 31, 2023
Last Update Posted:
Apr 3, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by MED-EL Elektromedizinische Geräte GesmbH
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 3, 2023