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Status Telemetry for Cochlear Implantations

Prospective Study of Status Telemetry for Cochlear Implantations

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06223724
Acronym
PATHOS
Enrollment
20
Registered
2024-01-25
Start date
2023-10-25
Completion date
2024-10-01
Last updated
2024-01-29

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

Conditions

Sensorineural Hearing Loss

Brief summary

Cochlear implants (CIs) are well-established neuroprosthesis used to restore hearing for patients with partial or complete deafness. However, the audiological outcomes of these implants can vary widely, and one reason for this is suboptimal electrode placement. The gold standard for measuring electrode positions is computed tomography (CT) scans, but they are expensive and expose patients to additional radiation, which is especially harmful for children. This study investigates an alternative approach using impedance telemetry data to estimate electrode positions without exposing patients to radiation. For this purpose, an extended telemetry version of a CE-certified cochlear implant software is used. The advanced impedance telemetry software can measure impedance subcomponents with improved measurement resolution that could be used for more accurate estimation of electrode insertion depth using specially designed estimation software. Ultimately, the investigators want to demonstrate the potential to improve audiological outcomes of cochlear implant recipients without exposing them to additional radiation.

Interventions

DEVICESTOP

Software to measure impedance telemetry data

DEVICEMAESTRO

Software to measure impedance telemetry data

Sponsors

Insel Gruppe AG, University Hospital Bern
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Informed Consent signed by the subject * Subjects scheduled for CI surgery according to clinical routine * Subjects who will receive a cochlear implant of the MED-EL portfolio (FLEX series arrays) * No radiological contraindications * Stated willingness to comply with all study procedures for the duration of the study

Exclusion criteria

* Lack of compliance with any inclusion criteria * Subjects incapable of giving informed consent * Age under 18 years * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Linear error of electrode insertion depth estimationAt the first post-operative CT scan according to conventional clinical routine (+0-4weeks)Linear error (in mm) in impedance-based estimation of cochlear implant electrode insertion depth compared to ground truth from CT scans.

Secondary

MeasureTime frameDescription
Intra-operative progression of impedance subcomponentsDuring cochlear implantation (day 0)Intra-operative measurement of access resistance and polarization impedance measured by the STOP software at several positions of the electrode array in the cochlea (stepwise insertion). The results will be expressed in kOhm (kΩ).
Post-operative progression of electrode insertion depth estimationRecordings will be made during cochlear implant surgery (day 0) and at three follow-up visits (+2weeks, +4weeks, +12weeks).Post-operative cochlear implant electrode insertion depth estimation using a phenomenological model based on access resistance and polarization impedance measured by the STOP software after full insertion of the electrode array. The results will be expressed in kOhm (kΩ).
Angular error of electrode insertion depth estimationAt the first post-operative CT scan according to conventional clinical routine (+0-4weeks)Angular error (in degrees) in impedance-based estimation of cochlear implant electrode insertion depth using a phenomenological model compared to ground truth from CT scans.

Countries

Switzerland

Contacts

Primary ContactStephan Schraivogel, MSc
stephan.schraivogel@unibe.ch+41 31 632 76 15
Backup ContactWilhelm Wimmer, Prof.
wilhelm.wimmer@tum.de

Outcome results

None listed

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