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NOT YET RECRUITING
NCT07081542
NA

Comparative Analysis of Hearing Outcomes: Robotic vs. Manual Insertion of Cochlear Implants

Sponsor: AdventHealth

View on ClinicalTrials.gov

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.

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

32

Start Date

2026-01-01

Completion Date

2027-01-31

Last Updated

2026-01-02

Healthy Volunteers

No

Interventions

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.

Locations (1)

AdventHealth Celebration

Kissimmee, Florida, United States