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COMPLETED NA

Perimodiolar Implant Performance in Adults With Low-Frequency Residual Hearing

NCT04741009 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the feasibility study is to investigate hearing performance (audiometry and speech perception) using the CI632 in a group of adults (n=15) with low-frequency residual hearing who meet inclusion criteria.

Interventions

  • DEVICE CI632 Slim Modiolar Electrode

Study Locations (4)

Ohio

  • Cleveland Clinic — Cleveland
  • University Hospitals — Cleveland

Massachusetts

  • UMass Memorial Medical Center — Worcester

Missouri

  • Midwest Ear Institute — Kansas City

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2021-12-16
Est. Completion 2025-06-16
Phase NA

Sponsor

Cochlear

43 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04741009

The ClinicalTrials.gov registry entry for NCT04741009 describes a study currently listed as completed. 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 10 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 Sensorineural Hearing Loss appearing as the primary indexed condition, and to 1 intervention — of which CI632 Slim Modiolar Electrode 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: NCT04741009 reports 4 study locations spanning 3 distinct geographic areas — top geographies include Ohio, Massachusetts, Missouri. 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 NCT04741009 about?

NCT04741009 is a clinical study titled "Perimodiolar Implant Performance in Adults With Low-Frequency Residual Hearing". The purpose of the feasibility study is to investigate hearing performance (audiometry and speech perception) using the CI632 in a group of adults (n=15) with low-frequency residual hearing who meet inclusion criteria.

What is the current status of trial NCT04741009?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2021-12-16. Estimated completion is 2025-06-16.

What conditions does trial NCT04741009 study?

This clinical trial studies the following conditions: Sensorineural Hearing Loss, Low-Frequency Residual Hearing. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04741009?

The interventions under investigation include: CI632 Slim Modiolar Electrode (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04741009?

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 NCT04741009 being conducted?

This trial has 4 study locations across Massachusetts, Missouri, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial