Clinical Performance Evaluation of 3D Ear Canal Scanning Technology

Completed

Conditions studied: Ear Mold Impression Procedure

In brief

Study participants will undergo ear canal impressions in a standard of care protocol utilizing two methodologies: 3D ear scanning using a commercially-available ear scanning device, and conventional silicone impression material. The elapsed time of each procedure will be captured for each participant, and the average duration of the two methodologies will be compared.

Key facts

Study ID

NCT05000047

Run by

Sonova AG

People needed

30

Starts

2021-05-17

Expected to finish

2021-07-15

Last updated by the study team

2023-06-01

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Hearing impairment (any degree, type, and configuration)

You may not qualify if…

• Absent or abnormal external auditory canal and/or external auditory meatus.
• Positive history of external/middle ear surgery.

Where it is running

• Phonak Audiology Research Center — Aurora, Illinois, United States

Full record on ClinicalTrials.gov

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