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Cross-sectional Evaluation of the Subjective Performance and Satisfaction With Ponto Sound Processors (BC112)

Oticon Medical logo

Oticon Medical

Status

Completed

Conditions

Hearing Loss, Conductive
Hearing Loss
Hearing Loss, Unilateral

Treatments

Device: Ponto Sound processor

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

The study is a non-interventional, observational, cross-sectional, study on users of Ponto sound processors. The purpose of this study is to evaluate subjectively assessed hearing performance and satisfaction with Oticon Medical's sound processors fitted with the Genie Medical fitting software.

Full description

The study is a non-interventional, observational, cross-sectional, study on users of Ponto sound processors. The purpose of this study is to evaluate subjectively assessed hearing performance and satisfaction with Oticon Medical's sound processors fitted with the Genie Medical fitting software. Subjects fitted with one or two Ponto sound processors will be invited to participate in an online survey. The survey contains questions about the subjectively experienced performance and satisfaction of the device. The survey can be filled out on computer, tablet or mobile phone and should take the participants about 10 minutes to fill out.

Enrollment

170 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Online consent form filled out Has been fitted with at least one Ponto Sound Processor

Exclusion criteria

No exclusion criteria

Trial design

170 participants in 1 patient group

Ponto Users
Description:
Users that have been fitted with a Bone Anhcored Sound Processor, Ponto
Treatment:
Device: Ponto Sound processor

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Marianne Philipsson

Data sourced from clinicaltrials.gov

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