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Hearing Loss, Unilateral clinical trials

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NCT ID: NCT03281967 Completed - Mixed Hearing Loss Clinical Trials

Clinical Survey of Minimally Invasive Ponto Surgical Technique (MIPS)

Start date: June 9, 2017
Phase: N/A
Study type: Interventional

The objective of the study is to compare the outcomes after a surgical procedure with minimally invasive Ponto surgery (MIPS, test group) and tissue preservation surgery (control) for placing Oticon Medical Ponto implants and abutments.

NCT ID: NCT03149484 Completed - Clinical trials for Hearing Loss, Unilateral

Use of RM Technology in Pediatric BAI Recipients

Start date: May 2, 2017
Phase:
Study type: Observational

The purpose of this research study is to learn about the hearing outcomes of children with conductive hearing loss who are treated with bone conductive devices and their outcomes with remote microphone technology.

NCT ID: NCT02963974 Completed - Clinical trials for Hearing Loss, Unilateral

Cochlear Implantation in Pediatric Cases of Unilateral Hearing Loss

CIPUHL
Start date: April 20, 2017
Phase: N/A
Study type: Interventional

This feasibility study evaluates whether children with unilateral, moderate to profound sensorineural hearing loss experience an improvement in speech perception, hearing in noise, localization, and quality of life with a cochlear implant as compared to an unaided listening condition.

NCT ID: NCT02722330 Completed - Clinical trials for Single Sided Sensorineural Deafness

Evaluation of Cochlear Baha 5 SuperPower Sound Processor on the Baha Attract System

Start date: April 2016
Phase: N/A
Study type: Interventional

The aim of this clinical investigation is to evaluate objective and subjective hearing performance with the Cochlear Baha 5 SuperPower Sound Processor on the Baha Attract System, compared to the unaided hearing performance. Comparison of audiological test results with the same sound processor on a Baha Softband will also be performed. Short term safety parameters will be collected.

NCT ID: NCT02534298 Completed - Clinical trials for Unilateral Hearing Loss

Functional Magnetic Resonance Imaging Study of the Central Auditory System After Single Sided Deafness

SSD
Start date: April 2015
Phase: N/A
Study type: Interventional

The objective is to study the relation between the reorganization of the central auditory system, and the psychophysical deficits in binaural hearing in subjects with single sided deafness.

NCT ID: NCT02269124 Completed - Clinical trials for Unilateral Hearing Loss

Use of Amplification in Children With Unilateral Hearing Loss

UHL
Start date: October 1, 2014
Phase: N/A
Study type: Interventional

Unilateral hearing loss (UHL) in children has been demonstrated to have a negative impact on quality of life, school performance and behavior. Despite this knowledge, it remains unclear how to best manage this common problem. There has been much debate regarding this issue with many programs recommending preferential seating in the classroom and use of a frequency-modulated (FM) system to amplify the teacher's voice in the classroom (conventional measures), and others recommending these accommodations in addition to use of a hearing aid for amplification (amplification). There is very limited research to support or refute the efficacy of a hearing aid in improving measurable academic, behavioral, or quality-of-life (QOL) outcomes in children with UHL. We propose a study evaluating the impact of hearing aid use in school-aged children (ages 6-12 years) with mild to moderately severe UHL. In this study, subjects will be randomized to receive either conventional measures or conventional measures plus amplification. After a three month period, the groups will be reversed, with each subject serving as their own control. Outcome measurements will include patient reported disease-specific QOL reported by patients, parents, and teachers using validated survey instruments at regular intervals throughout the study period.

NCT ID: NCT01715948 Completed - Unilateral Deafness Clinical Trials

Comparison of BAHA and CROS Hearing Aid in Single-Sided Deafness

Start date: January 2013
Phase: N/A
Study type: Interventional

People with single-sided deafness (SSD) have significant hearing loss in one ear and normal or near normal hearing in the other ear. Those living with SSD experience several communication difficulties, particularly when listening to speech in the presence of background noise. This problem is worse in situations where the noise is on the side of the good ear and the speech is on the side of the poor ear. The Bone-Anchored Hearing Aid (BAHA) and the Contralateral Routing of Signals (CROS) hearing aid are two devices designed to improve hearing in people who have significant hearing loss in one ear only. The BAHA is a surgically implanted device which also includes an external processor; sounds from the poor ear are transmitted to the good ear through skull vibrations. The CROS does not involve surgery; instead a hearing aid is fitted behind each ear, and the sounds on the side of the poor ear are wirelessly transmitted to the good ear. The majority of previous studies comparing the BAHA to the CROS have used older CROS models with basic technology and a wire along the neck to send sounds from the poor ear to the good ear. There is a lack of studies comparing newer digital wireless CROS hearing aids to the BAHA. The current research will compare the effect of the BAHA and CROS hearing aid on speech perception scores when listening to speech in quiet and in noise. The research will also investigate patients' reported benefits with each device during everyday situations. In order to compare the BAHA and CROS, individuals who already have been implanted with a BAHA will be given a trial period with a new wireless digital CROS hearing aid. The research hypothesis states that the CROS hearing aid will be as equally beneficial or greater than the BAHA in improving hearing and patient benefit. If the findings support the hypothesis that the CROS offers just as much benefits as the BAHA, or is an even better alternative, more patients may choose to avoid surgery and decide to receive a CROS hearing aid instead.

NCT ID: NCT01108406 Completed - Hearing Loss Clinical Trials

Long Term Safety of the Sonitus SoundBite System

Start date: April 2010
Phase: N/A
Study type: Interventional

The objective of this study is to assess the long-term safety and quality of life improvement of the Sonitus SoundBite Hearing System.

NCT ID: NCT00977314 Completed - Clinical trials for Unilateral Hearing Loss

Bone Conduction Auditory Performance Via the Tooth for Single-Sided Deafness

Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of using bone conduction via the teeth to treat Single-Sided Deafness (SSD).

NCT ID: NCT00201617 Completed - Unilateral Deafness Clinical Trials

Efficacy of the Bone-anchored Hearing Aid for Unilateral Deafness

Start date: July 2004
Phase: N/A
Study type: Observational

The purpose of this 3-year prospective investigation is to examine the short-term and long-term (1 year)efficacy of the bone-anchored hearing aid (BAHA) in adults with single sided deafness