Quest Sound Recover (SR2) vs. Venture SR2

Sonova

Status

Completed

Conditions

Hearing Loss

Treatments

Device: hearing aid

Study type

Interventional

Funder types

Industry

Identifiers

NCT02895477

Sonova2016_10

Details and patient eligibility

About

Goal of this study is to determine the benefit of an improved feature on a new hearing aid platform.

To investigate the improvements of this feature is compared on a new and older hearing aid platform. The obtained results will be used for future improvement for this feature. This feature should improve the speech understanding and speech recognition of the hearing aid user.

Enrollment

23 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Informed Consent as documented by signature (Appendix Informed Consent Form)
Ability to fill in a question conscientious
Healthy outer ear (w/o previous surgical procedures)
Sensorineural symmetric hearing loss (HL)
N4 to N7 (degree of HL)

Exclusion criteria

Contraindications to the MD in this study, e.g. known hypersensitivity or allergy to the investigational product,
Limited mobility and not in the position to attend weekly appointments
Limited ability to describe listening impressions/experiences and the use of the hearing aid
Inability to produce a reliable hearing test result when pure tone audiometry is attempted by the audiologist
Massively limited dexterity
Known Psychological problems
Central hearing problems