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MED-EL HEARING SOLUTIONS (MEHS): AN OBSERVATIONAL STUDY — MEHS  

Hearing Loss Clinical Trial

Official title:
MED-EL HEARING SOLUTIONS (MEHS): AN OBSERVATIONAL STUDY

Clinical Trial Summary

This Registry represents a non-interventional systematic collection of clinical data in which prospective data from children and adults are collected as fully anonymized data sets, derived from original clinical records on appropriately informed subjects. This is a patient-outcomes Registry for subjects of any age who are provided in routine clinical practice with one or more MED-EL hearing devices. The Registry aims to collect data for hypothesis generation on subject device use, auditory performance, quality of life and health-related utilities, across different types of implantable and non-implantable hearing devices from MED-EL company. Subjects will be evaluated with a set of standardized tests and questionnaires prior to implantation or prior to initial device activation (baseline) and at follow-up intervals according to the clinical practice.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05668338
Study type Observational [Patient Registry]
Source MED-EL Elektromedizinische Geräte GesmbH
Contact Jasmine Rinnofner
Phone +43 57 788 1694
Email jasmine.rinnofner@medel.com
Status Recruiting
Phase
Start date June 26, 2017
Completion date December 2028
View Details
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