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Deafness Unilateral clinical trials

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NCT ID: NCT05073796 Completed - Deafness, Bilateral Clinical Trials

Cochlear Implant Electrostimulation and the Influence on the Vestibular Organ

Start date: September 9, 2020
Phase: N/A
Study type: Interventional

There is evidence that the sensor function of the utricle in patients with bilateral labyrinthine dysfunction (bilateral vestibulopathy) may improve balance under the influence of high frequency basal stimulation of the cochlea. The aim of the study is to measure the possible co-stimulation of the utricle (which is determined by the SVV) by tonotopic (frequency-specific) cochlear stimulation and thus to objectify whether the stimulation of the auditory nerve in CI patients also leads to an unavoidable co-stimulation of the vestibular system.

NCT ID: NCT04738968 Active, not recruiting - Deafness Unilateral Clinical Trials

Cochlear Implantation for Young Single-sided Deaf Children

CICADE
Start date: January 2015
Phase: N/A
Study type: Interventional

Children with profound sensorineural unilateral hearing loss (UHL) lag behind in spoken language, cognition, spatial hearing, and academic performance compared to normal hearing (NH) children. Until recently children with UHL were not remediated, thereby assuming that the normal ear would provide sufficient sensory cues for speech understanding. However, this is not true. Because of the difference between the two ears they have difficulty localizing sounds and understanding speech in noise. Such auditory deprivation leads to more global changes in neurocognitive function. It is expected that a cochlear implant in the deaf ear will provide the necessary cues for hearing with two ears. The main objective of this research project is to fundamentally investigate language, cognitive, and spatial/binaural hearing longitudinally in children with unilateral deafness who receive a cochlear implant and age-matched peers.

NCT ID: NCT03289845 Completed - Deafness Unilateral Clinical Trials

Clinical Survey of Oticon Medical Ponto BHX Implant

Start date: November 5, 2015
Phase: N/A
Study type: Interventional

Investigation of stability of the BHX implant in adult patients indicated and counselled for a bone anchored hearing aid system. Patients are followed according to clinical practice for a total of 12 months in the study. Stability of the implant is evaluated by implant stability quotient.