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Quality of Life With Bone Conduction Hearing Device

NCT03864731 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2025-05-13

No results posted yet for this study

Summary

The aim of this study is to compare the audiological and quality of life performance patients have with an ADHEAR (adhesive bone conduction device) compared to no hearing device.

Conditions

  • Conductive Hearing Loss

Interventions

DEVICE

Bone conduction device (ADHEAR)

adhesive bone conduction device

Sponsors & Collaborators

  • Medical University of Vienna

    lead OTHER

Principal Investigators

  • Valerie Dahm, MD · MUW

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
13 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-25
Primary Completion
2024-07-31
Completion
2024-10-31

Countries

  • Austria

Study Locations

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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 NCT03864731 on ClinicalTrials.gov