Trials / Not Yet Recruiting
Not Yet RecruitingNCT07081542
Comparative Analysis of Hearing Outcomes: Robotic vs. Manual Insertion of Cochlear Implants
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (estimated)
- Sponsor
- AdventHealth · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This research study is evaluating two different methods of cochlear implant (CI) insertion - robotic-assisted insertion and manual insertion - to better understand how they affect hearing outcomes. Participants in this study will be randomly assigned to receive their cochlear implant using one of these two techniques. Both methods are performed in a standard operating room by qualified surgeons, and both are considered safe and approved for use. The main goal is to compare how well participants hear one year after surgery based on the insertion method used. The study will also look at things like surgical time, inner ear health, and how the hearing nerve responds. All participants will receive the same type of cochlear implant device and follow-up care. This study may help guide future surgical techniques and improve outcomes for individuals receiving cochlear implants.
Conditions
- Sensorineural Hearing Loss
- Bilateral Hearing Loss
- Cochlear Implantation
- Hearing Disorders
- Hearing Disorders and Deafness
- Inner Ear Disorders
- Hearing Impairment
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | IotaSoft Robotic Insertion System | The IotaSoft robotic insertion device is an FDA-approved tool designed to provide precise and controlled insertion of the cochlear implant electrode array to minimize trauma during implantation. |
| PROCEDURE | Manual Cochlear Implant Insertion | Standard surgical technique for manually inserting the cochlear implant electrode array. This method reflects the current standard of care without the assistance of robotic tools. |
Timeline
- Start date
- 2026-01-01
- Primary completion
- 2027-01-31
- Completion
- 2027-01-31
- First posted
- 2025-07-23
- Last updated
- 2026-01-02
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT07081542. Inclusion in this directory is not an endorsement.