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NCT05274178 · ClinicalTrials.gov registry record · NA

Effect of Hearing Aid Labeling on Speech Understanding Measures

A NA study of Hearing Loss, sponsored by Sonova.

Completed
Registry status
NA
Development phase
20
Enrollment target
1
Study location

NCT05274178 is a NA study of Hearing Loss that has completed, run by Sonova. The registered enrollment target is 20 participants, below the 6,121-participant average among 58 other Hearing Loss trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05274178, a NA study of Hearing Loss, has completed, sponsored by Sonova.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

New and experienced hearing aid users will be fit with two hearing devices. One will be labeled as an OTC (Over-The-Counter) device, the other will be labeled as a Prescriptive (i.e. professionally fit) device. Both devices will be generically programmed for a mild to moderate hearing loss. An objective speech in noise test will be completed with both devices.

Conditions Studied

Hearing Loss

Interventions

  • DEVICE Audeo P hearing aid labeled as "Prescriptive"
  • DEVICE Audeo P hearing aid labeled as "OTC"

Study Locations (1)

Illinois

  • Sonova US - Aurora

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2022-05-26
Est. Completion 2022-06-16
Phase NA

Sponsor

Sonova

29 total trials

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What the Registry Record Tells You About NCT05274178

The ClinicalTrials.gov registry entry for NCT05274178 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 6,121-participant average among 58 other Hearing Loss trials with a reported enrollment target (100% lower). The listed sponsor is Sonova, which has 29 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hearing Loss appearing as the primary indexed condition, and to 2 interventions - of which Audeo P hearing aid labeled as "Prescriptive" is the first listed.

NCT05274178 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT05274178 about?

NCT05274178 is a clinical study titled "Effect of Hearing Aid Labeling on Speech Understanding Measures". New and experienced hearing aid users will be fit with two hearing devices. One will be labeled as an OTC (Over-The-Counter) device, the other will be labeled as a Prescriptive (i.e. professionally fit) device. Both devices will be generically programmed for a mild to moderate hearing loss. An objec...

What is the current status of trial NCT05274178?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2022-05-26. Estimated completion is 2022-06-16.

What conditions does trial NCT05274178 study?

This clinical trial studies the following conditions: Hearing Loss.

What interventions are being tested in trial NCT05274178?

The interventions under investigation include: Audeo P hearing aid labeled as "Prescriptive" (DEVICE), Audeo P hearing aid labeled as "OTC" (DEVICE).

Who is sponsoring clinical trial NCT05274178?

This trial is sponsored by Sonova, which has 29 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05274178 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.