Post-Market Clinical Investigation of the IotaSOFT Insertion System (ACE)

iotaMotion

Status: Enrolling

Conditions: Cochlear Implantation; Hearing Loss, Cochlear; Hearing Loss, Sensorineural

Treatments: Device: Cochlear Implantation with Robotic-Assisted Insertion System

Study type: Observational

Funder types: Industry

Identifiers

NCT06664697

ICI2401

Details and patient eligibility

About

The purpose of the proposed study is to evaluate the continued safety of the iotaSOFT Insertion System when used by a surgeon to assist with inserting a CI electrode array in one ear per subject

Full description

available iotaSOFT Insertion System when used per intended use for insertion of a cochlear implant electrode array in subjects 12 years and older. The purpose of the study is to collect additional safety data in retrospective and prospective subjects. The primary object of the study is to demonstrate post-market safe use of the commercially available iotaSOFT Insertion System. The secondary objective of the study is to define procedural characteristics including device deficiencies, electrode array insertion speed, rate of tip fold-over, and objective measures of cochlear implant functionality to demonstrate effective use of the commercially available iotaSOFT Insertion System.

Enrollment: 50 estimated patients

Sex: All

Ages: 12+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Candidates with sensorineural hearing loss who received or will receive unilateral or bilateral cochlear implantation according to indications for use with FDA approved cochlear implant devices, as listed below:

   1. Advanced Bionics HiFocus SlimJ
   2. Cochlear Slim Straight
   3. MED-EL Flex 24 and 28

2. Age 12 years or older at the time of CI surgery.

3. Willingness to participate in the study and able to comply with the follow-up visit requirements.

Exclusion criteria

1. Prior cochlear implantation in the ear to be implanted.
2. Ossification or any other cochlear anomaly that might prevent complete insertion of the electrode array or present an increased risk of aberrant insertion.
3. Craniofacial abnormality, temporal squamosal skull thickness less than 3mm, major cochlear lesions (e.g., fibrosis, fracture, or ossification), or cochlear malformations.
4. Deafness due to lesions of the acoustic nerve or central auditory pathway.
5. Diagnosis of auditory neuropathy.
6. Active middle-ear infection or tympanic membrane perforation in the presence of active middle ear disease.
7. Absence of cochlear development.
8. Additional medical concerns that would prevent participation in evaluations as determined by the investigator.
9. Unrealistic expectations on the part of the subject, regarding the possible benefits, risks, and limitations that are inherent to the procedure and investigational device.
10. Non-native English speakers who are unable to read, understand and/or speak English for completion of required procedures
11. Planned or current participation in a clinical study of an investigational device or drug.
12. Must not fit the definition of a vulnerable subjects, as per FDA regulations 21 CFR Parts 50 and 56

Trial design

50 participants in 2 patient groups

Retrospective

Description:

Retrospective Review of patient records

Treatment:

Device: Cochlear Implantation with Robotic-Assisted Insertion System

Prospective

Description:

Prospective data collection of subjects receiving a cochlear implant with robotic-assisted cochlear implant

Treatment:

Device: Cochlear Implantation with Robotic-Assisted Insertion System