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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01805167
Other study ID # 12-AOI-06
Secondary ID 2012-A01374-39
Status Recruiting
Phase N/A
First received February 22, 2013
Last updated March 5, 2013
Start date February 2013
Est. completion date February 2014

Study information

Verified date February 2013
Source Centre Hospitalier Universitaire de Nice
Contact Nicolas GUEVARA, Dr
Email guevara.n@chu-nice.fr
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santé
Study type Interventional

Clinical Trial Summary

Differences in speech-understanding and the quality of the subjective perception among cochlear implant patients (Digisonic SP) depends on numerous factors. The electrical field distribution (interaction between electrodes) could also explain the disparity of the performances? The objective of our study was to quantify the influence of the electrical field interactions between the channels of stimulation according to the vocal performances of the implanted subjects, for various subjective levels of electric stimulation.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date February 2014
Est. primary completion date February 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Subject of French language

- Subject with a moderate bilateral sensorineural hearing loss, severe to profound

- Sensorineural hearing loss post-lingual (after onset of language acquisition)

- Subject paired with the implant Neurelec (Appendix 1) for more than 9 months

- Subject has received an appropriate setting under usual clinical follow-up

- Elderly 18 to 75 years

- Subject giving consent

Exclusion Criteria:

- Sensorineural hearing loss pre-lingual

- Deafness following a meningitis, or neurodegenerative diseases

- Illiteracy

- Pregnant women

- Subject blind

- Subject enjoying a measure of legal protection

- Subject incapable of giving consent

- Subject vulnerable

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
Electrophysiological study of the interindividual variability of vocal performance


Locations

Country Name City State
France CHU de Nice Nice

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quantify the interactions between electrical stimulation channels based vocal performance of implanted subjects, for different subjective levels of electrical stimulation. The vocal performance will be noted in percentage of voice recognition in the silence and in the noise.
And the electric interaction between the channels of stimulations will be estimated by the measure of the refractory period of the circuits of the hearing system with the PEAEP after stimulations of electrodes of intermediate situation in the cochlée (electrodes 11, 12 and 13)
At the inclusion - Day 0 No
Secondary Comparative study of PEAEP (Auditory Evoked Potentials Early electric) in vocal performance Collection of the PEAEP after stimulation of 4 different electrodes distributed on the totality of door-electrode: generally, electrodes 4, 7, 10 and 13 will be stimulated. The amplitudes and the latencies of the waves II, III and V will be analyzed and compared with the vocal performances. At the inclusion - Day 0 No
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