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Clinical Trial Summary

This early feasibility study aims to collect pilot data on impedance measurements in real-world environments and to collect real-world and difficult listening situations and the factors impacting this, reflecting situations the subjects encounter during their daily life outside of the clinic. Improving the monitoring of both aspects may lead to improvements in monitoring and personalising the fitting to optimise hearing outcomes for persons with a cochlear implant.


Clinical Trial Description

This is a feasibility, prospective, multi-country, multi-centre, cross-sectional interventional clinical investigation in adults with a CE labelled cochlear implant. No Randomisation nor blinding to avoid bias is applicable in this study since there is no comparator. Subjects will attend two scheduled study visits over a two-month study period. At and in between study visits, subjects will undergo hearing assessments and safety monitoring. The subjects will perform daily impedance test tasks and complete a questionnaire in order to obtain the first primary endpoint, i.e. characterization of Daily Impedance Fluctuations. Furthermore, the subjects will do EMA tasks to obtain the secondary objectives to capture daily-life, real-world listening environments and challenging listening environments. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06173687
Study type Interventional
Source Cochlear
Contact Taike Bruyneel
Phone 003216795564
Email tbruyneel@cochlear.com
Status Recruiting
Phase N/A
Start date January 29, 2024
Completion date October 2024

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