Evaluation of Subjective Ratings on a New Sound Processor and Compatible Products

Status

Withdrawn

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02934373

Enrollment

Registered

2016-10-17

Start date

Unknown

Completion date

Unknown

Last updated

2016-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hearing Loss

Brief summary

Clinical study designed to collect user feedback from Cochlear Implant recipients on a new Sound Processor System

Interventions

DEVICEA New Sound Processor

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

1 Years to 100 Years

Healthy volunteers

Yes

Inclusion criteria

1. 12 months old or older 2. Implanted with a CI24RE (Freedom implant) or later implant in at least one implanted ear 3. Use of the CP810, CP920 or CP910 sound processor 4. Willingness to participate in and to comply with all requirements of the protocol

Exclusion criteria

1. Unrealistic expectations on the part of the subject, regarding the possible benefits, risks and limitations that are inherent to the procedure and prosthetic device 2. Additional disabilities or illnesses that would prevent participation in evaluations or compromise the integrity of the investigation or quality of data collected 3. Nucleus 22 or Nucleus 24 Implant in ear to be fitted with the investigational device

Design outcomes

Primary

Measure	Time frame
Subjective rating with a new sound processor compared to ratings with each subjects own processor	3 months

Countries

Belgium, United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026