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Characterisation of Low Frequency Hearing and Vestibular Function in Patients Undergoing Cochlear Implantation

Characterisation of Low Frequency Hearing and Vestibular Function in Patients Undergoing Cochlear Implantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06021132
Enrollment
39
Registered
2023-09-01
Start date
2022-05-01
Completion date
2028-02-28
Last updated
2025-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hearing Loss, Bilateral, Hearing Loss, Sensorineural

Keywords

Cochlear implant, Residual hearing, Hearing preservation

Brief summary

The study will follow a cohort of CI-candidates becoming CI-user, till two years postoperative. A through-out assessment of both their audiological and vestibular status will be carried out at multiple fixed timepoints over 2 years, evaluating both subjective (patients reported) and objective outcomes over time. For the audiological part of the study both pure-tone and speech audiometry results will be held against the patient perceived benefit of the treatment as assessed by the questionnaires NCIQ and SSQ-12. The vestibular part of the study will evaluate the function of the SCCs and the sacculus. This is will be put in concert with functional tests of the vestibular system, and the patient perceived outcome measure DHI. Correlations between vestibular and audiological performances will be examined. A collection of specific hypotheses will be tested by predefined statistical methods.

Interventions

DEVICEcochlear implant

Insertion of a electrode into the cochlear with the aim of providing deaf and severe hearing handicapped with the ability to hear speech.

Sponsors

Aalborg University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults (At or above 18 years of age and capable of giving an informed consent) * Cochlear implant candidacy * Profound bilateral post-lingual hearing loss * Proficiency in Danish * Expected ability to participate on both all pre- and postoperative examinations * No previous CI experiences

Exclusion criteria

* Later abandonment of CI candidacy * Blindness or visual handicap compromising eye movement evaluation * Distinct neck mobility handicap hindering either vHIT- or cVEMP examination * Patient reluctance, such as consistent no-show or cancellations of appointments * CI-surgery before preoperative evaluation could be obtained * Simultaneous bilateral cochlea implantation. * Sequential CI within the follow-up period

Design outcomes

Primary

MeasureTime frameDescription
Anticipated increase in patient reported outcome measures+24 months from last inclusion. Expected to be complete in juli 2025.The preoperative status will be held against their performance at 6, 12 and 24 months. Yet the performance at 6 months will also be held against status at 24 months
Test-retest assessment of vestibular screening batteryConducted before cochlear implantation in all patients.Double examination using commercial video head impulse test system and cervical vestibular evoked myogenic potentials.
Anticipated increase in speech audiometric performances+24 months from last inclusion. Expected to be complete in juli 2025.The preoperative status will be held against their performance at 6, 12 and 24 months. Yet the performance at 6 months will also be held against status at 24 months

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026