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Clinical Trial Summary

The objective of this feasibility study is to obtain preliminary safety and efficacy data associated with cochlear implantation in individuals with severe to profound sensorineural hearing loss contralateral to an ear with normal, or near-normal, hearing. The hypothesis is that restoration of hearing in the deafened ear will result in improved speech perception in the treated ear and advantages related to restoration of hearing to both ears.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01670006
Study type Interventional
Source Cochlear
Contact
Status Completed
Phase N/A
Start date October 2012
Completion date February 2016

See also
  Status Clinical Trial Phase
Not yet recruiting NCT01933386 - Evaluation of Benefit for Treatment of Single Sided Deafness (SSD) Between Two Bone Conduction Prosthetic Devices; Osseointegrated Implant Versus Maxilla Anchored Removable Oral Appliance ("SoundBite") Phase 4
Active, not recruiting NCT01445977 - SoundBite Hearing System Long Term Multi Site Patient Use Study N/A
Recruiting NCT01807559 - SoundBite Hearing System 24 Month Multi Site Patient Use Study N/A
Recruiting NCT05775367 - Cochlear Implants in Young Children With SSD N/A
Recruiting NCT03327194 - Use of ADHEAR, a Non-Implantable Bone Conduction Hearing System, in Children With Single Sided Deafness and/or Conductive Hearing Loss N/A
Completed NCT02064478 - Clinical Survey of Oticon Medical Ponto Implants and a Surgical Technique With Tissue Preservation N/A
Completed NCT02966366 - Tinnitus Treatment With Cochlear Implant in Single Sided Deafness N/A