Hybrid L24 New Enrollment Post Approval Study (HNE)

  • End date
    Mar 11, 2024
  • participants needed
  • sponsor
Updated on 11 March 2022


This study evaluates the long term safety and effectiveness of the Nucleus Hybrid L24 Implant in a group of newly implanted adults.

Condition High Frequency Sensorineural Hearing Loss
Treatment Nucleus Hybrid L24 Implant
Clinical Study IdentifierNCT02379819
Last Modified on11 March 2022


Yes No Not Sure

Inclusion Criteria

Ear to Be Implanted
Normal to moderate hearing loss in the low frequencies with severe to profound mid to high frequency hearing loss in the ear to be implanted
CNC word recognition of 10-60% in the ear to be implanted
Contralateral Ear
Moderately severe to profound mid to high frequency hearing loss in the contralateral ear
CNC word recognition equal to or better than that in the ear to be implanted but not more than 80% correct

Exclusion Criteria

non-native English speaker
unwilling to comply with the test protocol
unrealistic expectations regarding the intervention
duration of sever to profound hearing loss of 30 years or greater
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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