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Safety and Effectiveness of Cochlear Implantation in an Expanded Adult Population
NCT06293482 · View on ClinicalTrials.gov ↗
Study Summary
This study aims to evaluate the safety and efficacy of cochlear implantation for adults with bilateral sensorineural hearing loss who currently do not meet the FDA-approved indications for cochlear implantation. Following cochlear implantation, participants will complete speech perception assessments and questionnaires over the course of seven visits.
Conditions Studied
Interventions
- DEVICE Cochlear™ Nucleus® System
Study Locations (9)
Arizona
- Barrow Neurological Institute — Phoenix
- Centre for Neurosciences — Tucson
California
- Pacific Neuroscience Institute — Santa Monica
Florida
- University of Miami — Coral Gables
Indiana
- Indiana University — Indianapolis
Missouri
- Midwest Ear Institute — Kansas City
New York
- New York University — New York
Ohio
- Cleveland Clinic — Cleveland
Pennsylvania
- University of Pennsylvania Hospitals — Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-09-17 |
| Est. Completion | 2028-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06293482
The ClinicalTrials.gov registry entry for NCT06293482 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cochlear, which has 43 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Hearing Loss, Sensorineural appearing as the primary indexed condition, and to 1 intervention — of which Cochlear™ Nucleus® System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06293482 reports 9 study locations spanning 8 distinct geographic areas — top geographies include Arizona, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06293482 about?
NCT06293482 is a clinical study titled "Safety and Effectiveness of Cochlear Implantation in an Expanded Adult Population". This study aims to evaluate the safety and efficacy of cochlear implantation for adults with bilateral sensorineural hearing loss who currently do not meet the FDA-approved indications for cochlear implantation. Following cochlear implantation, participants will complete speech perception assessment...
What is the current status of trial NCT06293482?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2024-09-17. Estimated completion is 2028-10.
What conditions does trial NCT06293482 study?
This clinical trial studies the following conditions: Hearing Loss, Sensorineural, Hearing Loss, Bilateral. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06293482?
The interventions under investigation include: Cochlear™ Nucleus® System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06293482?
This trial is sponsored by Cochlear, which has 43 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06293482 being conducted?
This trial has 9 study locations across Arizona, California, Florida, Indiana, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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