Actively Recruiting
MED-EL HEARING SOLUTIONS (MEHS): AN OBSERVATIONAL STUDY
Led by MED-EL Elektromedizinische Geräte GesmbH · Updated on 2026-02-19
100
Participants Needed
8
Research Sites
700 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
Official Title
MED-EL HEARING SOLUTIONS (MEHS): AN OBSERVATIONAL STUDY
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children and adults planned or submitted for unilateral or bilateral implantation using simultaneous or sequential procedures
- Children and adults planned or submitted for unilateral or bilateral treatment with a non-implantable MED-EL device
- Users of cochlear implants, electric-acoustic devices, bone conduction implants, middle ear implants, or other MED-EL hearing solutions, unilateral, bilateral, or bimodal
- Signed written informed consent for data collection for Registry purposes
You will not qualify if you...
- Not meeting any of the inclusion criteria
- Any condition that the Investigator believes increases risk or prevents full compliance with Registry procedures
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 8 locations
1
Katholisches Klinikum Bochum
Bochum, Germany, 44787
Actively Recruiting
2
Universitätsklinik Carl Gustav Carus - Klinik und Poliklinik für Hals-, Nasen- und Ohrenheilkunde
Dresden, Germany, 01307
Actively Recruiting
3
Universitätsklinikum der Goethe-Universität
Frankfurt, Germany, 60590
Actively Recruiting
4
Sektion Otologie und Neuro-Otologie UNI-Klinikum Heidelberg
Heidelberg, Germany, 69120
Actively Recruiting
5
Klinikum der Universität München Campus Großhadern
München, Germany, 81377
Actively Recruiting
6
Evangelisches Krankenhaus Oldenburg
Oldenburg, Germany, 26122
Actively Recruiting
7
Klinik und Poliklinik für Hals-, Nasen-, Ohrenheilkunde, Kopf- und Halschirurgie "Otto Körner"
Rostock, Germany, 18057
Actively Recruiting
8
Universitätsklinikum Tübingen, Klinik für Hals-, Nasen- u. Ohrenheilkunde, Plastische Operationen
Tübingen, Germany, 72076
Actively Recruiting
Research Team
J
Jasmine Rinnofner
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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