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A Comparative Clinical Investigation of Two Hearing Instrument Digital Signal Processing

NCT04374851 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 19

Last updated 2021-01-07

No results posted yet for this study

Summary

The purpose of this study is to show that the performance of the new digital signal processing system is better than the system used in the currently CE marked devices. Speech in narrowband noise and acceptable levels of noise should be improved with the new system, and speech understanding overall should not be negatively affected. There should be no artefacts or unwanted noises caused by the new system.

Conditions

Interventions

DEVICE

Polaris miniRITE BTE

The Polaris device is programmed with computer software to match the Hearing loss of the participant.

DEVICE

Viron miniRiTE BTE

The Viron Hearing device is programmed with computer software to match the Hearing loss of the participant.

Sponsors & Collaborators

  • Bernafon AG

    lead INDUSTRY

Principal Investigators

  • Barbara Simon, AuD · Bernafon AG

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-08-03
Primary Completion
2020-11-30
Completion
2020-11-30

Countries

  • Switzerland

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 NCT04374851 on ClinicalTrials.gov