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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04882800
Other study ID # SRF-72
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 8, 2021
Est. completion date June 15, 2021

Study information

Verified date July 2022
Source Sonova AG
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluating the efficacy and effectiveness of an advancement in the fitting characteristics of extended wear technology with the commercially available device as a comparator.


Description:

A interventional study in which participants will be fit with the commercially available device in one ear and the experimental device in the opposite ear. After two weeks, the devices will be switched so that the participant has worn each device in each ear for a total of 2 weeks. Participants will be blinded as to which device they are wearing in each ear. Comfort and sound quality will be assessed for each device prior to removing from ears.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date June 15, 2021
Est. primary completion date May 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Mild, Moderate and Moderate Severe Hearing loss - Previous extended wear technology users who rejected or cancelled trials due to discomfort, feedback, migration, or poor sound quality due to fit issues Exclusion Criteria: - Participants who can only wear a size XXS (extra-extra small) extended wear device - asymmetrical hearing loss - other diagnosis that may cause hearing fluctuation - inability to tolerate physical fit of Lyric devices - inability to be seen for four lab visits

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Lyric extended wear hearing aid device A
Current commercially available extended wear hearing aid
Lyric extended wear hearing aid with fitting modification device B
Extended wear hearing aid with fitting modifications

Locations

Country Name City State
United States Main Line Audiology Consultants Narberth Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Sonova AG

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Subjective Questionnaire of Comfort Subjective ratings of comfort of each device in the ear, on a scale from 0 (very comfortable) to 10 (very uncomfortable/painful). No statistical analysis was planned for this measure. Two weeks after fitting device A in right ear/device B in left ear (Day 14 of study), and two weeks after fitting device A in left ear/device B in right ear (Day 28 of study-final appointment)
Primary Subjective Ratings of Occlusion With Both Devices Subjective ratings on how plugged participants' ears felt with each device in ear,on scale from 0 (not at all) to 10 (extremely plugged/cannot tolerate) Two weeks after fitting device A in right ear/device B in left ear (Day 14 of study), and two weeks after fitting device A in left ear/device B in right ear (Day 28 of study-final appointment)
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