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Hearing Loss, Cochlear clinical trials

View clinical trials related to Hearing Loss, Cochlear.

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NCT ID: NCT06218966 Not yet recruiting - Clinical trials for Hearing Loss, Sensorineural

Usability of the Intracochlear Catheter INCAT - a Feasibility Study

INCAT
Start date: January 15, 2024
Phase: N/A
Study type: Interventional

This is a feasibility study for a inner ear catheter which will be used to apply steroids to the inner ear. It will be used on nearly deaf patients during their surgery, when they receive an implant that will restore the hearing. Treatment with steroids will improve the maintenance of residual hearing, which will be tested during and after the surgery.

NCT ID: NCT03101917 Not yet recruiting - Clinical trials for Hearing Loss, Cochlear

Microtable® Method for Cochlear Implantation Investigational Device Exemption (IDE)

Start date: July 1, 2024
Phase: N/A
Study type: Interventional

The Microtable® Microstereotactic Frame and Drill Press and Associated Method for Cochlear Implantation consists of a patient-customized microstereotactic frame which targets the cochlea. The intended use of the device in this early feasibility study is to surgically access the cochlea, allowing placement of an intra-cochlear electrode array for cochlear implantation, thereby providing a less invasive surgical option than currently performed. Compared to traditional cochlear implantation (CI) surgery, the investigators hypothesize that the minimally invasive, image-guided approach may offer the following benefits: (1) shorter procedure time including shorter general anesthesia time, (2) less tissue removal potentially eliminating post-operative mastoid bone depression, decreased post-operative patient discomfort, and quicker wound healing, (3) better chance of preservation of taste secondary to preservation of the chorda tympani nerve, and (4) standardization of electrode placement potentially allowing more consistent placement within the scala tympani sub-compartment of the cochlea which has been shown to be associated with improved post-operative audiological performance. This early feasibility study will focus on the advantages of the new technology to the patient. Advantages to the healthcare delivery system will be examined during the pivotal study phase.