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Pupillometry Techniques Usage to Quantify the Programming Parameters Effect in the Auditory Effort in Zti Opticon Cochlear Implant Adult Users

F

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla

Status

Unknown

Conditions

Unilateral Sensorineural Hearing Loss
Bilateral Sensorineural Hearing Loss

Treatments

Device: Neuro Zti cochlear implant and Neuro 2 sound processor

Study type

Observational

Funder types

Other

Identifiers

NCT05300230
FIS-ZTI-2019-01

Details and patient eligibility

About

The aim of this study is to establish the connection between the cochlear implant programming parameters with the auditory effort associated with the speech perception evaluated by pupillometry techniques in different audiometric conditions.

Enrollment

25 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Users willing to participate in the study with signature and date of the Informed Consent.
  • Age between 18 and 70 years old.
  • At least 6 months experience with the Neuro Zti implant and Neuro 2 processor.
  • Unilateral, bilateral and bimodal users.
  • Basic understanding of oral and written Spanish.
  • Normal or corrected vision.

Exclusion criteria

  • Speech or language disorder.
  • Added comorbidities or cognitive dysfunction.
  • Not approval to participate in the study or absence in some of the programmed sessions for the Cochlear Implant.

Trial design

25 participants in 1 patient group

Patients with Zti Opticon Cochlear Implant
Description:
Patients that are users of Neuro Zti and Neuro 2 processor with a minimum of 6 months of habituation after the implementation.
Treatment:
Device: Neuro Zti cochlear implant and Neuro 2 sound processor

Trial contacts and locations

1

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Central trial contact

Amparo Callejón Leblic

Data sourced from clinicaltrials.gov

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