Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05793580
Other study ID # VSB_longterm_Rennes_study
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2008
Est. completion date September 1, 2018

Study information

Verified date March 2023
Source MED-EL Elektromedizinische Geräte GesmbH
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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).


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).


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date September 1, 2018
Est. primary completion date September 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
France CHU Rennes Rennes

Sponsors (1)

Lead Sponsor Collaborator
MED-EL Elektromedizinische Geräte GesmbH

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tonal audiometry Pure-tone audiograms preoperatively
Primary Tonal audiometry Pure-tone audiograms at 1 month post-implantation
Primary Tonal audiometry Pure-tone audiograms at 3 months post-implantation
Primary Tonal audiometry Pure-tone audiograms at 6 months post-implantation
Primary Tonal audiometry Pure-tone audiograms at 12 months post-implantation
Primary Tonal audiometry Pure-tone audiograms at 60 months post-implantation
Secondary Word recognition in quiet Speech recognition test of disyllabic words (Fournier lists). preoperatively
Secondary Word recognition in quiet Speech recognition test of disyllabic words (Fournier lists). at 1 month post-implantation
Secondary Word recognition in quiet Speech recognition test of disyllabic words (Fournier lists). at 3 months post-implantation
Secondary Word recognition in quiet Speech recognition test of disyllabic words (Fournier lists). at 6 months post-implantation
Secondary Word recognition in quiet Speech recognition test of disyllabic words (Fournier lists). at 12 months post-implantation
Secondary Word recognition in quiet Speech recognition test of disyllabic words (Fournier lists). at 60 months post-implantation
Secondary Word recognition in noise 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°. preoperatively
Secondary Word recognition in noise 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°. at 1 month post-implantation
Secondary Word recognition in noise 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°. at 3 months post-implantation
Secondary Word recognition in noise 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°. at 6 months post-implantation
Secondary Word recognition in noise 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°. at 12 months post-implantation
Secondary Word recognition in noise 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°. at 60 months post-implantation
Secondary Speech reception threshold Speech reception threshold to have 50% of intelligibility on disyllabic words. preoperatively
Secondary Speech reception threshold Speech reception threshold to have 50% of intelligibility on disyllabic words. at 1 month post-implantation
Secondary Speech reception threshold Speech reception threshold to have 50% of intelligibility on disyllabic words. at 3 months post-implantation
Secondary Speech reception threshold Speech reception threshold to have 50% of intelligibility on disyllabic words. at 6 months post-implantation
Secondary Speech reception threshold Speech reception threshold to have 50% of intelligibility on disyllabic words. at 12 months post-implantation
Secondary Speech reception threshold Speech reception threshold to have 50% of intelligibility on disyllabic words. at 60 months post-implantation
See also
  Status Clinical Trial Phase
Completed NCT03807713 - Clinical Study of Minimally Invasive Ponto Surgical Technique (MIPS) - Design Iteration N/A
Completed NCT04320407 - Osia CPT Code Study N/A
Completed NCT02304692 - Clinical Survey of Different Abutment Topologies N/A
Active, not recruiting NCT05628285 - Evaluation of a Hearing Device for Transmitting Sound to the Inner Ear N/A
Completed NCT03374787 - Evaluation of Sound Processor for a Transcutaneous System N/A
Completed NCT03086135 - Clinical Performance of a New Implant System for Bone Conduction Hearing N/A
Withdrawn NCT01264510 - Evaluation of the Effectiveness of Bone-anchored Hearing Aids (Baha) Phase 4
Completed NCT03281967 - Clinical Survey of Minimally Invasive Ponto Surgical Technique (MIPS) N/A
Completed NCT03143257 - Ambispective Clinical Evaluation of Sophono™
Completed NCT02274129 - Clinical Survey of Oticon Medical Healing Cap N/A
Completed NCT05000931 - Osia 2 Pediatric Expansion Study N/A
Completed NCT02064478 - Clinical Survey of Oticon Medical Ponto Implants and a Surgical Technique With Tissue Preservation N/A
Completed NCT03848910 - Subject´s Preference Regarding Hearing Performance and Functionality Using a New Sound Processor N/A
Completed NCT01780025 - Objective Measures in Implantable Hearing Devices