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Hearing Loss, Sensorineural clinical trials

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NCT ID: NCT01184248 Completed - Clinical trials for Sensorineural Hearing Loss

The Effect of Sound Stimulation on Pure-tone Hearing Threshold

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

The purpose of this study is to investigate if sound stimulation could improve pure-tone hearing threshold. In the late 1990s, researchers discovered that acoustic stimuli slow progressive sensorineural hearing loss and exposure to a moderately augmented acoustic environment can delay the loss of auditory function. In addition, prolonged exposure to an augmented acoustic environment could improve age-related auditory changes. These ameliorative effects were shown in several types of mouse strains, as long as the acoustic environment was provided prior to the occurrence of severe hearing loss. In addition to delaying progressive hearing loss, acoustic stimuli could also protect hearing ability against damage by traumatic noise. In particular, a method called forward sound conditioning (i.e., prior exposure to moderate levels of sound) has been shown to reduce noise-induced hearing impairment in a number of mammalian species, including humans. Interestingly, recent report has suggested that low-level sound conditioning also reduces free radical-induced damage to hair cells, increases antioxidant enzyme activity, and reduces Cox-2 expression in cochlea, and can enhance cochlear sensitivity. Specifically, increased cochlear sensitivity was observed when distortion product otoacoustic emissions (DPOAEs) and compound action potentials (CAPs) were measured. In addition to forward sound conditioning, backward sound conditioning (i.e., the use of acoustic stimuli after exposure to a traumatic noise) has been shown to protect hearing ability against acoustic trauma and to prevent the cortical map reorganization induced by traumatic noise. Based on the results of animal studies, the investigators conducted a human study in 2007 and observed that sound stimulation could improve hearing ability. On average, the pure-tone hearing threshold decreased by 8.91 dB after sound stimulation for 2 weeks. In that study, however, the investigators observed only the hearing threshold changes by sound stimulation. To verify the previous ameliorative effect of sound stimulation, the investigators included a control period in this study.

NCT ID: NCT01092910 Completed - Clinical trials for Mild to Severe Sensorineural Hearing Loss

Esteem Totally Implantable Hearing System

Start date: January 2008
Phase: N/A
Study type: Interventional

To evaluate the safety and efficacy of the Esteem Totally Implantable Hearing System in subjects suffering from mild to severe hearing loss.

NCT ID: NCT01054378 Completed - Neck Pain Clinical Trials

Diaphragmatic Movement Before and After Stellate Ganglion Block : A Ultrasonographic Study

Start date: January 2010
Phase: Phase 4
Study type: Interventional

The temporary diaphrgmatic dysfunction will occur after stellate ganglion block(SGB) and will be easily detected by M-mode ultrasonography

NCT ID: NCT00925236 Completed - Clinical trials for Fechtner Syndrome (Disorder)

Phenotypic and Genotypic Identification and Characterization of MYH9-related Constitutional Thrombocytopenia

MAGIC-MYH9
Start date: August 2009
Phase: N/A
Study type: Observational

The research involves the establishment of a cohort including as much as possible cases of macrothrombocytopenia related to a "MYH9 syndrome" and the study of mutations and polymorphisms of MYH9 gene in all these patients. As MYH9 syndrome is an autosomal dominant disorder, patients should be heterozygous for a MYH9 gene mutation. The main goal of our project is looking for correlations between genotype and phenotype. It is planned to characterize the phenotype and genotype of a cohort of patients, including family members that will be addressed during the study in order to better understand the platelet disorder and improve the epidemiological knowledge of MYH9 syndrome. The data will be recorded in a database.

NCT ID: NCT00802425 Completed - Hearing Loss Clinical Trials

Efficacy of AM-111 in Patients With Acute Sensorineural Hearing Loss

Start date: December 2008
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine whether AM-111 is effective in the treatment of acute inner ear hearing loss (acute sensorineural hearing loss, ASNHL).

NCT ID: NCT00787189 Completed - Clinical trials for Sensorineural Hearing Loss

Study of Low Level Laser Therapy and Word Recognition in Hearing Impaired Individuals

Start date: August 2007
Phase: N/A
Study type: Interventional

The purpose of this clinical study is to determine the effectiveness of low level laser light therapy when applied around the head and ears in improving unaided word recognition in ears with sensorineural hearing loss.

NCT ID: NCT00724347 Completed - Clinical trials for Hearing Loss, Sensorineural

PC-Based Rehabilitation of Auditory Function

CINT
Start date: July 2008
Phase: N/A
Study type: Interventional

Many older subjects experience difficulty in understanding speech in noisy environments. Part of this problem is related to changes that occur in the ear with age and compromise the hearing of high-pitched sounds. Another part of the problem with speech understanding relates to changes with age in the neural circuits of the brain that process different speech sounds. Evidence suggests that these changes in neural circuits are particularly large if hearing loss is present. Thus, while hearing aids may help compensate for hearing deficits by amplifying speech sounds, additional treatment is necessary to restore optimal neural connections in the brain so that speech sounds can be accurately distinguished from each other. We are developing PC-based training programs in an attempt to restore optimal neural connections. The current randomized trial will evaluate whether two months of training to improve the ability to discriminate different consonant sounds in noise will also improve the understanding of continuous speech and enhance auditory memory and other high-level auditory functions.

NCT ID: NCT00678899 Completed - Clinical trials for Sensorineural Hearing Loss

Evaluation of the Nucleus Hybridâ„¢ L24 Cochlear Implant System

Start date: April 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy associated with the provision of acoustic and electric sound processing to individuals who demonstrate significant residual low-frequency hearing and profound high-frequency (above 1500 Hz) sensorineural hearing loss. Delivery of acoustic-electric stimulation will be provided by the Nucleus Hybrid L24 cochlear implant system.

NCT ID: NCT00594061 Completed - Clinical trials for Hearing Loss, Sensorineural

Iowa/Nucleus 10/10 mm and Nucleus Freedom Feasibility Study

Start date: December 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether the Iowa/Nucleus 10/10 mm in one ear, in conjunction with a Nucleus Freedom implant in the other ear can provide useful binaural hearing in pediatric subjects who have bilateral severe to profound hearing loss and meet the criteria for cochlear implantation. The Iowa/Nucleus 10/10 mm cochlear implant has a short, 10 mm electrode array that it is inserted only into the more basal region of the cochlea. Unlike a conventional cochlear implant, the Iowa/Nucleus 10/10 mm is expected to preserve the regions of the cochlear partition that are apical to the electrode, thus leaving them available for possible future advances in the field of otolaryngology and hearing devices, such as mammalian hair cell regeneration techniques or improved implantable hearing devices. The Iowa/Nucleus 10/10 mm will be implanted in the contralateral ear from the Nucleus Freedom electrode array as a means of providing bilateral stimulation of auditory pathways while preserving the middle and apical regions of the scala media.

NCT ID: NCT00589511 Completed - Clinical trials for Sensorineural Hearing Loss

Nucleus Freedom Cochlear Implant System Pediatric Post-approval Study

Start date: October 2006
Phase: N/A
Study type: Observational

The objective of this multisite study is to evaluate the performance of the Nucleus Freedom cochlear implant system in a large population of sequentially implanted pediatric subjects.