Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Cochlear
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
At least three months of experience with the cochlear implant.
Implanted with the CI600 series (CI612, CI622, CI632) or CI500 series (CI512, CI522, CI532) cochlear implant.
Able to be programmed with ACE (Advanced Combination Encoder), a fixed pulse width (PW) MAP with a maximum PW of 50 us per channel and with ≥ 18 enabled channels on the sound processor MAP.
Fluent speaker in the language used to conduct the study procedures, as determined by the investigator.
Willing and able to provide written informed consent and to comply with all requirements of the protocol.
You may not be if
Participants programmed with an acoustic component in the tested ear.
Additional health factors, known to the investigator, that would prevent or restrict participation in the evaluations, including significant visual impairment and/or dexterity issues.
Unable or unwilling to comply with the requirements of the clinical investigation as determined by the investigator.
Investigator site personnel directly affiliated with this study and/or their immediate families; immediate family is defined as a spouse, parent, child, or sibling.
Cochlear employees or employees of Contract Research Organizations or contractors engaged by Cochlear for the purposes of this investigation.
Current participation, or participation in another interventional clinical study/trial in the past 30 days, involving an investigational drug or device (unless Cochlear sponsored and determined by investigator or Sponsor to not impact this investigation).
