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

Study acronym: MEHS
StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Primary and study completion dates: Dec 2028 to Dec 2030
    • Primary endpoints: 8 to 9
    v6
  2. Site contacts updated at 1 of 8 sitesv5
  3. Site contacts updated at 1 of 8 sitesv4
  4. Re-verified, no change to tracked fieldsv3
  5. Site details revised at 1 of 8 sitesv2
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT05668338
Lead Sponsor MED-EL Elektromedizinische Geräte GesmbH
Conditions
(from sponsor)		 Hearing Loss
Related terms Hearing Loss
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov