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

NCT05356221 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 170

Last updated 2025-08-17

Study results available
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Summary

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.

Conditions

  • Hearing Loss
  • Hearing Loss, Conductive
  • Hearing Loss, Unilateral

Interventions

DEVICE

Ponto Sound processor

Bone Anchored Hearing solution fitted to compensate for the subjects hearing loss

Sponsors & Collaborators

  • Oticon Medical

    lead INDUSTRY

Principal Investigators

  • Marianne Philipsson · Oticon Medical

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-11
Primary Completion
2024-09-01
Completion
2024-09-01
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05356221 on ClinicalTrials.gov