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Active, not recruiting Not applicable Interventional

Safety and Efficacy of a Drug Eluting Slim Modiolar Electrode Array

ClinicalTrials.gov ID: NCT06598059

Public ClinicalTrials.gov record NCT06598059. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 10:04 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Pivotal, Prospective, Multicentre, Single-arm Study Evaluating the Safety and Efficacy of a Dexamethasone Eluting Slim Modiolar Electrode Array (EA32D).

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This clinical study will test a new type of cochlear implant known as CI632D. This experimental cochlear implant has been designed to slowly release a drug called dexamethasone. Dexamethasone works to ease inflammation and reduce tissue injury, which is common after any type of surgery. The goal is to learn if the dexamethasone in the CI632D implant lessens these reactions inside the ear following surgery and if this makes the implant work as well, or even better, in improving hearing than what would be expected with a standard cochlear implant. The study will be conducted in adults with sensorineural hearing loss, a type of hearing loss caused by damage to the inner ear or auditory nerve (the nerve that carries sound signals from the ear to the brain). The study participants will receive the CI632D experimental implant and will complete tests to see how well they are hearing and how well the implant is working.

Study identification

NCT ID
NCT06598059
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Cochlear
Industry
Enrollment
56 participants

Conditions and interventions

Conditions

Interventions

Device · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 3, 2025 (Actual)
Primary completion
Feb 2, 2026 (Actual)
Completion
Sep 2026 (Estimated)
Last update posted
Mar 2, 2026

2025 – 2026

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
9
Facility City State ZIP Site status
UCLA Medical Center Los Angeles California 90095 —
Rocky Mountain Ear Center Englewood Colorado 80113 —
University of Iowa Iowa City Iowa 52242 —
Henry Ford Health Detroit Michigan 48202 —
Washington University St Louis Missouri 63141 —
New York Eye and Ear Infirmary New York New York 10010 —
NYU Langone Health New York New York 10017 —
Northwell Health Long Island Jewish Medical Center New York New York 11042 —
University Hospitals Cleveland Ohio 44106 —
Oregon Health & Science University Portland Oregon 97239 —
Medical University of South Carolina Charleston South Carolina 29425 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06598059, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 2, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06598059 live on ClinicalTrials.gov.

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