The HEARing CRC
Melbourne, Victoria, 3053, Australia
NCT Number: NCT02905305
In an effort to further preserve residual acoustic hearing after cochlear implantation, it may be beneficial to incorporate anti-inflammatory agents into the electrode array for passive elution over a time course after implantation. This study aims to assess the ease and effectiveness of such an electrode design, and to assess the preliminary safety of use of such a device in the post-operative period. This study is a first-time-in-human study of the investigational device.
In the first instance, the aim of the current investigation is to obtain first experience in use of a Combined Device in the adult clinical population, and to assess tools and techniques that may be considered in future clinical studies of similar devices.
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Notify Me18 year–85 year
All sexes
Interventional
Not applicable
Melbourne, Victoria, 3053, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The Combined Device consists of a standard cochlear implant receiver-stimulator coupled to a Contour Advance electrode loaded with a controlled dose of dexamethasone base.
Standard Contour Advance electrode
Time frame: During surgery
Questionnaire used to obtain surgical feedback from experienced cochlear implant surgeons regarding the electrode design, and ease and effectiveness of surgery, when using the Combined Device as compared to the Contour Advance electrode
Time frame: Monitoring over 24 months
Monitoring of device related adverse events that occur during the study period, to assess the preliminary safety of the Combined Device
Time frame: Testing over 24 months
Time frame: Testing over 24 months
The Hearing Cooperative Research Centre
Other
Pilot Evaluation of Combined Investigational Device: CI4CID With Controlled Dosage of Dexamethasone
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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