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Deafness clinical trials

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NCT ID: NCT02203305 Completed - Clinical trials for Asymmetric Hearing Loss

Cochlear Implantation in Cases of Single-Sided Deafness

CI in SSD
Start date: October 2014
Phase: N/A
Study type: Interventional

The primary goal of this project is to determine whether subjects with Single-Sided Deafness (SSD) experience an improvement in speech perception, localization, and quality of life with a cochlear implant as compared to an unaided listening condition.

NCT ID: NCT02189798 Terminated - Hearing Loss Clinical Trials

Implantation of the HiRes90K™ Advantage Cochlear Implant With HiFocus™ Mid-Scala and Development of a Combined Electric and Acoustic Stimulation Technology in Adults With Partial Deafness

Start date: October 21, 2014
Phase: N/A
Study type: Interventional

The purpose of this feasibility study is to evaluate whether low-frequency acoustic hearing sensitivity can be preserved in newly implanted adults with partial deafness (considerable low frequency acoustic hearing profiles with severe-to-profound high frequency sensorineural hearing loss) using the HiResolution™ 90K™ Advantage cochlear implant with the HiFocus™ Mid-Scala electrode to support the development of electro-acoustic stimulation technology (EAS).

NCT ID: NCT02154971 Completed - HIV Seropositivity Clinical Trials

Assessment of Age-related Hearing Loss in HIV-1 Patients

HELO
Start date: November 18, 2013
Phase:
Study type: Observational

The ageing process is known to be accelerated in HIV-infected patients, compared to the general population. Normal age-related hearing loss (presbyacusia) is a frequent phenomenon, affecting more than 70% of people above 65 years. It is believed to be mostly the consequence of a mitochondrial damage caused by oxidative stress. Risk factors for accelerated age-related hearing loss are present in many HIV-infected patients : chronic inflammation, smoking, diabetes, etc. The global aim is to measure the prevalence of presbyacusia in a well controlled HIV positive population in France, and to compare it to HIV negative controls matched for age and sex. 90 HIV positive patients and 90 age- and sex- matched HIV negative controls will undergo a screening for presbyacusia (pure-tone, speech and evoked-response audiometry). We expect to find an increased prevalence of presbyacusia in HIV-infected patients, as compared to controls matched for age and sex.

NCT ID: NCT02132130 Completed - Clinical trials for Unilateral Severe to Profound Hearing Loss OR Bilateral Severe to Profound Hearing Loss

Safety, Tolerability and Efficacy for CGF166 in Patients With Unilateral or Bilateral Severe-to-profound Hearing Loss

Start date: June 23, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of the study was to evaluate the safety, tolerability, and the potential ability of CGF166 delivered through IL-infusion to improve hearing. CGF166 is a recombinant adenovirus 5 (Ad5) vector containing a cDNA encoding the human Atonal transcription factor (Hath1).

NCT ID: NCT02122458 Completed - Hearing Impairment Clinical Trials

Blast Exposed Veterans With Auditory Complaints

Start date: August 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to study blast-exposed Veterans who report hearing handicap but show normal or near normal results on standard audiometric testing. The characteristics and nature of their auditory and auditory-related skills will be examined, along with whether coexisting PTSD contributes to the hearing problems of these Veterans. In a preliminary treatment study, a sub-sample of these Veterans will be fitted with mild-gain hearing aids to determine if they benefit from low-level amplification of high-frequency sounds.

NCT ID: NCT02114554 Recruiting - MELAS Syndrome Clinical Trials

Mitochondrial nt3243 A>G Mutation in Taiwan

Start date: January 2014
Phase: N/A
Study type: Observational

Mitochondrial diseases are multisystem disorders that present with a wide range of clinical manifestations. Mitochondrial DNA nt3243A>G mutation is one of the most common mutations seen in mitochondrial diseases. Syndromes associated with this mutation include mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS), maternally inherited diabetes and deafness (MIDD), myoclonic epilepsy with ragged red fibers (MERRF), and chronic progressive external ophthalmoplegia (CPEO). Clinical analyses of mitochondrial DNA nt3243A>G mutation from Taiwan remain scarce. The present study aims to investigate the clinical features and prognostic factors of patients with mt3243A>G mutation in Taiwan.

NCT ID: NCT02105441 Completed - Clinical trials for Severe Unilateral Sensorineural Hearing Loss

Cochlear Implantation Among Adults and Older Children With Unilateral or Asymmetric Hearing Loss

CI and SSD
Start date: March 2014
Phase:
Study type: Observational

Do adults and children over 7 years of age with unilateral or assymetric hearing loss benefit from cochlear implantation on the worst hearing side.

NCT ID: NCT02102256 Active, not recruiting - Clinical trials for Bilateral Cochlear Nerve Deficiency

A Safety Study of the Auditory Brainstem Implant for Pediatric Profoundly Deaf Patients

Start date: March 2014
Phase: Phase 1
Study type: Interventional

Current treatment options for bilateral profoundly deaf children, diagnosed with inner ear anatomical abnormalities, are limited and, in the case of absent cochleas, non-existent. An auditory brainstem implant (ABI) places an electrode close to the auditory nucleus in the brainstem. Children aged 2 - 5 who are not candidates for a cochlear implant, or who did not demonstrate benefit from a cochlear implant, will be implanted with an ABI and followed for 1 year for safety and a total of 3 years for preliminary efficacy. This is a feasibility study to determine the safety of the ABI.

NCT ID: NCT02096809 Completed - Clinical trials for Hearing Loss - Conductive

Stability of the Cochlear Baha BI300/BA400 Implant System Loaded From 1 Week Post-surgery

Start date: March 2014
Phase: N/A
Study type: Interventional

Objectives - To evaluate the safety of processor loading of the Cochlear BI300/BA400 implant system 1 week after implantation - To evaluate the short term soft tissue healing and the long term skin reaction, with the new Cochlear BI300/BA400 implant system using the linear incision without subcutaneous tissue reduction. - To produce reference data regarding the stability of the BI300/BA400 implant system. Study design: Prospective cohort study. Patients: 24 adults with anticipated normal skin and bone quality eligible for bone anchored implant surgery. Intervention: Loading of the sound processor one week after surgery Main outcome measures: Implant stability, soft tissue reaction, skin overgrowth, pain and numbness will be assessed. It is hypothesized that implant loading can be performed one week after surgery without any changes in implant stability, soft tissue reaction, skin overgrowth, pain or numbness around implant.

NCT ID: NCT02094625 Completed - Osteosarcoma Clinical Trials

NAC to Prevent Cisplatin-induced Hearing Loss

Start date: March 2016
Phase: Phase 1
Study type: Interventional

Cisplatin is a key chemotherapy agent for the treatment of multiple childhood cancers but causes permanent hearing loss. This study investigates the drug N-acetylcysteine (NAC) to determine the dose necessary to protect hearing and also how well tolerated NAC is when combined with chemotherapy.