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Quality Control of CE-Certified Phonak Hearing Aids - 2020_26

Quality Control of CE-Certified Phonak Hearing Aids - 2020_26

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04496791
Enrollment
24
Registered
2020-08-03
Start date
2020-06-01
Completion date
2020-08-07
Last updated
2020-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hearing Loss

Brief summary

Phonak Hearing Devices pass through different development and study phases. At an early stage, feasibility studies are conducted to investigate new algorithms, features and functions in an isolated manner. If the benefit is proven, their performance is then investigated regarding interdependency between all available algorithms, features and functions running in parallel in a hearing aid (pivotal/pre-validation studies) and, resulting from the pre-validation studies, they get optimized. Prior to product launch, the Phonak Hearing Systems get reviewed by a final quality control in terms of clinical trials. This is a validation study, investigating improved algorithms, features, functions and wearing comfort. This will be a clinical investigation which will be conducted mono centric at Sonova AG Headquarters based in Stäfa (Switzerland).

Detailed description

This study will investigate the combination of the features to determine if the audiological performance and quality of the new successor of the Marvel family shows an improved benefit over Phonak Audéo Marvel before going into the System Validation. Therefore this study will be a comparative study. The study will determine if hearing impaired users wearing the successor hearing aids, have better initial acceptance with the new precalculation, better sound quality and speech intelligibility, more clarity and loudness comfort in soft and loud environments compared to Phonak Marvel RIC (Receiver in channel) hearing aids. Another objective of the study is to compare the listening effort with the two different study devices.

Interventions

DEVICERIC (Receiver in Canal) hearing aid/ hearing instrument (HI)

HI is developed to support hearing impaired people in calm and complex situations and to be able to participate in communication

Sponsors

Sonova AG
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hearing Loss range: N3-N4 * experienced hearing aid user * willingness to wear behind the ear hearing aids * Informed Consent as documented by signature

Exclusion criteria

* the audiogram is not in the fitting range of the intended hearing aid * first time user * limited mobility and not in the position to attend weekly appointments in Stäfa (Switzerland) * participant is not able to describe experiences and hearing impressions * allergies against the material of the hearing aid

Design outcomes

Primary

MeasureTime frameDescription
Rating of the sound quality for the new and the comparative HI4 weeksSubjective rating of the overall satisfaction for sound quality by questionnaires for the new HI and the old comparative HI (%). The participants rates after one week home trial. The home trial is randomized. The questionnaire includes rating scales for the satisfaction. The participant has to rate it in percentage (100% = very satisfy, 0% = very unsatisfy)

Secondary

MeasureTime frameDescription
Speech intelligibility in noisy situations (only test device)4 weekEvaluating the speech intelligibility with the test device, using a speech in noise test, Oldenburger Satztest (OLSA) after the subject set the noise cancellation via an App on an individual limit. The results of the test are the word recognition score in SNR.
Speech intelligibility in quiet situations4 weekEvaluating and comparing the speech intelligibility in a quiet test situation of the test device and the Marvel device. Using the Reimtest nach Wallenberg und Kollmeier (WaKo ) (%).
Speech intelligibility in noisy situations4 weeksEvaluating and comparing the speech intelligibility in a noisy test situation of the test device and competitor. Using the OLSA (word recognition score)
Rating of sound quality1 weekSubjective rating of the overall satisfaction for sound quality by questionnaires for the new HI and the old comparative HI (%). The participants rates after the First Fit. The questionnaire includes rating scales for the satisfaction. The participant has to rate it in percentage (100% = very satisfy, 0% = very unsatisfy)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026