NCT05668338

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

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 100 (estimated)
• Sponsor: MED-EL Elektromedizinische Geräte GesmbH · Industry
• Sex: All
• Age: —
• Healthy volunteers: Not accepted

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.

Conditions

• Hearing Loss

Interventions

Type	Name	Description
DEVICE	Implantable or non-implantable MED-EL hearing solution	Receipt of an implantable or non-implantable MED-EL hearing solution

Timeline

• Start date: 2017-06-26
• Primary completion: 2030-12-01
• Completion: 2030-12-01
• First posted: 2022-12-29
• Last updated: 2026-02-19

Locations

8 sites across 1 country: Germany