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Hearing Loss, Sensorineural clinical trials

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NCT ID: NCT01793168 Recruiting - Clinical trials for Retinitis Pigmentosa

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

CoRDS
Start date: July 2010
Phase:
Study type: Observational [Patient Registry]

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access. Visit sanfordresearch.org/CoRDS to enroll.

NCT ID: NCT01781039 Recruiting - Clinical trials for Sensorineural Hearing Loss

Investigation of Anatomical Correlates of Speech Discrimination

Start date: January 2013
Phase:
Study type: Observational

Understanding speech is essential for good communication. Individuals with hearing loss and poor speech discrimination often have little success with hearing aids because amplifying sound improves audibility, but not clarity of the speech signal. The purpose of this study is to determine the relative importance of the sensory cells of the inner ear and auditory neurons on speech discrimination performance in quiet and in noise. This information may be used as a predictor of hearing aid benefit. The investigators expect to find decreased speech understanding ability resulting from both loss of sensory cells and the loss of auditory neurons.

NCT ID: NCT01749592 Completed - Clinical trials for Sensorineural Hearing Loss (Disorder)

Single-sided Deafness and Cochlear Implants

Start date: December 2012
Phase: N/A
Study type: Interventional

- As the left and right hemisphere are specialized for different auditory tasks, the proposed study aims at demonstrating different consequences of right or left-sided deafness for the affected individual. - Furthermore, the question should be answered if auditory deficits and plastic changes can be partially reversed by cochlear implantation of the deaf ear. - Multicenter, prospective, open, non-randomized clinical trial with 5 patients with right-sided and 5 patients with left-sided sensineural deafness. - Pre-operative: Audiometry, Sound Localization Audiometry, PET, EEG/MEG - Comparison of pre-operative investigations with 10 healthy subjects (age and gender matched control group) - Cochlea implantation - Follow-up Visits at 3, 6, 9 and 12 month post-operative: Audiometry, Sound Localization Audiometry, PET, EEG, Questionnaires - Trial with medical device

NCT ID: NCT01671176 Completed - Clinical trials for Conductive Hearing Loss

Wide Diameter Bone Anchored Implant Study

Start date: May 2012
Phase: N/A
Study type: Interventional

To assess implant stability, implant loss, adverse skin reactions, and Quality of Life Benefit following implantation of the Ponto 4.5mm Wide Diameter implant. Secondary: to determine the feasibility of fitting the sound processor 3 weeks after surgical implantation, and to investigate if the type of skin reactions following implantation could be related to the demographic data of subjects and the type of surgical technique used

NCT ID: NCT01655212 Terminated - Clinical trials for Sensorineural Hearing Loss

Congenital Cytomegalovirus: Efficacy of Antiviral Treatment in a Randomized Controlled Trial

CONCERT
Start date: June 2012
Phase: Phase 3
Study type: Interventional

The objective of the trial is to investigate whether early treatment with oral valganciclovir of infants with both congenital cytomegalovirus infection and sensorineural hearing loss can prevent progression of hearing loss.

NCT ID: NCT01621256 Completed - Hearing Loss Clinical Trials

Efficacy, Safety, and Tolerability of Ancrod in Patients With Sudden Hearing Loss

Start date: May 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether ancrod is effective and safe in the treatment of sudden sensorineural hearing loss (SSHL).

NCT ID: NCT01532713 Completed - Clinical trials for SSNHL(Sudden Sensory Neural Hearing Loss)

The Effect of Oxygen Administration on Regional Cerebral Oxygen Saturation (rSO2) in the Non-block Side After Stellate Ganglion Block

Start date: January 2012
Phase: N/A
Study type: Interventional

Stellate ganglion block (SGB) is known to increase blood flow to the innervation area of the stellate ganglion. Near infrared spectroscopy reflects changes of blood volume and allows continuous, non-invasive, and bedside monitoring of regional cerebral oxygen saturation (rSO2). Previous studies have shown the increment of the rSO2 on the block side from the baseline and the decrement of the rSO2 on the non-block side after SGB. Patients with cerebral vascular disease undergoing SGB might be at risk a decrease in cerebral blood flow in the non-block side. The investigators researched the effect of oxygen administration on rSO2 in the non-block side using a near infrared spectroscopy after SGB. 5 L/min oxygen was supplied via nasal cannula from 15 minutes after SGB. The rSO2 in the non-block side were measured before SGB and 5, 10, 15, 20, 25 and 30 minutes after SGB. The present study suggests that oxygen administration can increase the rSO2 of non-block side. In conclusion, it is our belief that oxygen supplement is helpful to the patient with cerebral vascular disease during SGB.

NCT ID: NCT01529333 Not yet recruiting - Clinical trials for Mixed Conductive and Sensorineural Hearing Loss, Bilateral

Middle-Ear Implant With MET V Transducer (Aka MET V System)

Start date: May 2012
Phase: N/A
Study type: Interventional

The purpose and objective of this study is to evaluate the safety and efficacy of the MET V System for the treatment of individuals with mixed hearing loss.

NCT ID: NCT01518920 Completed - Clinical trials for Hearing Loss, Sensorineural

A Study Of The Effects Of PF-04958242 In Subjects With Age-Related Hearing Loss

Start date: December 2011
Phase: Phase 1
Study type: Interventional

The objective of this study is to examine the safety, tolerability, and effects on hearing thresholds of two single doses of PF-04958242 and placebo in subjects with age-related hearing loss.

NCT ID: NCT01509287 Completed - Clinical trials for Donnai-Barrow Syndrome

Metabolic Screening in Patients With Donnai-Barrow Syndrome

Start date: March 2010
Phase:
Study type: Observational

This study focuses on the genetics and metabolism of Donnai-Barrow Syndrome (DBS).