Mi2000 Totally Implantable Cochlear Implant (Mi2000 TICI)

Hearing Loss, Sensorineural Clinical Trial

Official title:

Mi2000 Totally Implantable Cochlear Implant (Mi2000 TICI): Pivotal Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06459765
• Other study ID #: MED-EL_CRD_2021_02
• Status: Recruiting
• Phase: N/A
• Start date: June 2024
• Est. completion date: March 2025

Study information

• Verified date: June 2024
• Source: MED-EL Elektromedizinische Geräte GesmbH
• Contact: Florian Schwarze, PhD
• Phone: +4357788
• Email: studies[@]medel.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this clinical trial is to test the Mi2000 Totally Implantable Cochlear Implant in a population of candidates for a cochlear implant. The main question it aims to answer is, whether the device is able to improve speech perception compared to the pre-operative score.

Participants will undergo cochlear implantation and fitting, and will be asked to perform the following tests pre- and post-operatively:

• Word test in quiet

• Sentence test in noise

• Audiograms

• Health Utilities Index 2 and 3 (HUI2&3), a generic quality-of-life questionnaire

• Nijmengen Cochlear Implant Questionnaire (NCIQ), a disease specific quality-of life questionnaire

• Speech, Spatial and Qualities of Hearing Scale (SSQ12), a disease specific questionnaire

• Hearing Implant Sound Quality Index (HISQUI19), a sound quality questionnaire

Description:

Cochlear implants (CI) provide a large majority of recipients with a significant degree of speech understanding. However, CI systems rely on external audio processors to function. This can have several disadvantages: for instance, the hardware is exposed to external trauma and to the effects of head movement and gravity. The device is also put at risk by humid, dusty, or dirty conditions as well as by physical activities that lead to water exposure such as swimming or sports in general (e.g. perspiration).

In addition, some patients are concerned with the cosmetic appearance of the external parts which are visible (more so than modern behind-the-ear hearing aids), something that may not be desirable to many potential candidates.

This clinical investigation aims to collect confirmatory data on the use of the Mi2000 Totally Implantable Cochlear Implant system used in combination with compatible devices.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: March 2025
• Est. primary completion date: March 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Minimum age of eighteen (18) years at time of enrolment

• Bilateral sensorineural hearing loss with no or limited benefit from a hearing aid (>70 dB HL PTA4)

• Post-lingual onset of deafness

• No or limited benefit from hearing aids for less than 10 years and an expected benefit from cochlear implantation

• A maximum score of 50% on a word test in the language of the test centre in the ear to be implanted in the best aided condition

• Fluency in the test language with excellent proficiency, as appropriate to perform speech testing

• Functional auditory nerve

• General health condition, psychological and emotional condition deemed compatible with the treatment and tests performed in this study

• Pre-operative assessment according to the local professional standards

• Candidate is highly motivated and has realistic expectations about the expected benefit of the implant and shall understand the importance of returning to the implant centre for regular speech processor programming, assessment sessions and training

• Realistic expectations, as deemed appropriate by the implanting surgeon/implant board

• Evidence of up-to-date vaccinations against meningitis, as per recommendations by the applicable national body

• Signed and dated informed consent before the start of any study-specific procedure

Exclusion Criteria:

• Lack of compliance with any inclusion criterion

• Previously having received an implant on the location chosen for placing the cochlear implant

• Having received a hearing implant from another manufacturer than MED-EL on the contralateral ear

• Pre-existing condition known to necessitate MRI scans after implantation of the Mi2000 TICI

• Women being pregnant or nursing

• Women of childbearing age not reporting to use effective contraception

• The individual is known to be intolerant of the materials used in the implant or other required accessories including medical grade silicone, parylene C, titanium, platinum iridium, platinum, stainless chromate steel, thermoplastic elastomere (TPE-S), thermoplastic elastomere (SEBS), mixture of polycarbonate and acrylonitrile-butadiene-styrol polymer (PC/ABS), polyamide, liquid crystal polymer, silicone and polyurethane-coated silicone rubber)

• Absence of cochlear development

• The cause of deafness is non-functionality of the auditory nerve and/or the upper auditory pathway

• Medical contra-indications to middle ear and/or inner ear surgery, and/or anaesthesia

• External or middle ear infections are present

• The tympanic membrane is perforated in the ear to be implanted

• Anatomic abnormalities are present that would prevent appropriate placement of the stimulator housing in the bone of the skull, or prevent placement of the chosen electrode array into the cochlea (including ossification of the cochlea)

• The psychological status of the individual is unstable

• The individual has unrealistic expectations

• Acute cholesteatoma

• History of vestibular schwannoma

• Unstable Meniere's disease

• Auditory Neuropathy

• Epilepsy not responding to treatment

• Permanent inability and/or unwillingness to participation in post-operative care and rehabilitation

• Known intellectual disability and/or psychological diseases

• Participation in other pharmacological clinical trials within four weeks prior to enrolment

• Anything that, in the opinion of the Investigator, would place the subject at increased risk; preclude the subject's full compliance with or completion of the study

Related Conditions & MeSH terms

• Hearing Loss
• Hearing Loss, Sensorineural

Intervention

Device:
• Mi2000 TICI
Cochlear Implantation

Locations

Country	Name	City	State
Austria	AKH Wien	Wien
Belgium	UZA Antwerpen	Antwerp
Belgium	CHU Liège	Liège
Germany	LMU Munich	München	Bavaria
Germany	UKW Würzburg	Würzburg	Bavaria
Poland	The Institute of Physiology and Pathology of Hearing	Nadarzyn

Sponsors (1)

Lead Sponsor	Collaborator
MED-EL Elektromedizinische Geräte GesmbH

Countries where clinical trial is conducted

Austria,  Belgium,  Germany,  Poland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Word test in quiet	Word test in quiet	through study completion, an average of 6 months after first fitting
Other	Sentence Test in Noise	Oldenburg Matrix Test	3- and 6-months after first fitting
Other	Speech, Spatial, Quality of Hearing (SSQ12)	Speech, Spatial and Quality of hearing scale	through study completion, an average of 6 months after first fitting
Other	Hearing Implant Sound Quality Index (HISQUI)	Sound quality questionnaire	through study completion, an average of 6 months after first fitting
Other	Audiograms	Audiograms	through study completion, an average of 6 months after first fitting
Primary	Word Test in Quiet	Word test in quiet	Pre-op to 6 months after first fitting
Secondary	Health Utility Index Mark 3 (HUI3)	Generic Quality of Life	Pre-op to 6 months after first fitting
Secondary	Nijmegen Cochlear Implant Questionnaire (NCIQ)	Disease specific Quality of Life	Pre-op to 6 months after first fitting