Completed

Real-Ear Measurement (REM) and Test Box System Integration Into Fitting Software

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What is being tested

Real-Ear Measurement system integrated in hearing aid fitting software

Device
Who is being recruted

From 16 to 67 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other Study

Interventional
Study Start: September 2015
See protocol details

Summary

Principal SponsorPhonak AG, Switzerland
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2015

Actual date on which the first participant was enrolled.

Integration of the REM-verification within the fitting workflow will enable the hearing care professional to easily run real ear measurements. The purpose of the two study parts is to prove that an integrated cooperative system, consisting of fitting software and measurement system, matches desired responses for certain stimuli faster, more reliably and more precisely at the ear drums of hearing instrument wearers than current best practice processes.

Official TitleReal-Ear Measurement (REM) and Test Box System Integration Into Fitting Software
NCT02555462
Principal SponsorPhonak AG, Switzerland
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

205 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other Study

Some studies explore topics that don't fall into a specific category. These might include innovative research, new technologies, or emerging healthcare areas.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 16 to 67 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

2 inclusion criteria required to participate
Clean and healthy ear canal, eardrum and pinna

Ability to keep current position (of head and body) during a period of about 5 minutes while seated.

6 exclusion criteria prevent from participating
Ear infections

Ear wax in the ear

Hyperacusis

Pacemaker

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
The study arm goes through a comparative test run followed by a comparative hearing aid fitting.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Phonak AG

Stäfa, SwitzerlandOpen Phonak AG in Google Maps
CompletedOne Study Center