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Deafness clinical trials

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NCT ID: NCT02304692 Completed - Clinical trials for Conductive Hearing Loss

Clinical Survey of Different Abutment Topologies

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

This study is designed to compare two different surfaces of bone anchored hearing aid abutments in terms of bacterial colonization, inflammatory response and skin reactions.

NCT ID: NCT02294513 Completed - Alzheimer Disease Clinical Trials

Hearing Instruments in Alzheimer's Disease

HIAD
Start date: October 2014
Phase: N/A
Study type: Observational

There is a strong connection between hearing loss and cognitive impairment, particularly dementia, in old age. Worldwide, dementia affects approximately 5% of persons over the age of 65 years. Hearing loss is even more prevalent in old age, affecting an estimated one third of persons over the age of 65 years. Thus, there is likely a large degree of overlap between the impairments. Indeed, this overlap may influence older adults' everyday functioning, communication, social engagement and quality of life, as well as influencing the well-being of their family caregivers. This project will examine whether patients with hearing loss and Alzheimer's disease, the most common form of dementia, derive benefit the from hearing aids prescribed and fit to them following current best practice procedures in a geriatric audiology clinic. For the first time, a formal evaluation of the potential benefits of hearing aids for the patients' family caregivers will also be conducted.

NCT ID: NCT02274129 Completed - Clinical trials for Conductive Hearing Loss

Clinical Survey of Oticon Medical Healing Cap

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

This study investigates the use of a new healing cap which, through altered design and choice of material, has been improved when it comes to minimizing the risk of it falling off as well as increasing patient comfort.

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: NCT02264314 Completed - Hearing Loss Clinical Trials

Tele-educative Program to Improve Adherence to the Use of Hearing Aids in Patients With Hearing Loss

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

Hearing loss is the third most common chronic condition in over 65 years people, it is estimated that 77.8% of older adults suffer from it. However, there are reports of adherence to the use of hearing aids of only to 40%. The objective of this project is to measure the effectiveness of a tele-educative intervention to improve adherence to the use of hearing aids. A randomized controlled trial was performed. The active branch consists of the implementation of an educational program called Active Communication Education, consisting of 4 sessions with a trained rehabilitator. Participants will be also monitored by telephone headset use by personnel trained for three months. The control arm will consist of the usual care received by these patients. All participants will be assessed at home at 3, 6, 9, and 12 months after randomization.

NCT ID: NCT02259595 Completed - Hearing Loss Clinical Trials

Study to Determine the Safety, Tolerability, and Pharmacokinetic Profile of HPN-07 and HPN-07 Plus NAC

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

This study is a single-center, randomized, placebo-controlled, double-blind, single ascending dose escalation study to determine the safety, tolerability, and PK profile of oral administration of HPN-07 in single doses to approximately 32 healthy male and female subjects between 18 and 55 years of age. Subjects will receive single oral doses of the study drug. The primary endpoint of this trial is to establish the safety and tolerability of HPN-07 and HPN-07 plus N-acetylcysteine (NAC).

NCT ID: NCT02257983 Completed - Clinical trials for Noise-induced Hearing Loss

Protective Effects of EPI-743 on Noise-Induced Hearing Loss

Start date: October 31, 2014
Phase: Phase 2
Study type: Interventional

If effective, administration of EPI-743 should have protective effects against temporary noise-induced hearing loss.

NCT ID: NCT02204618 Completed - Clinical trials for Auditory Processing Disorder, Central

Cochlear Implantation in Single Sided Deafness and Asymmetrical Hearing Loss: a Cost/Utility Study.

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

The investigators assume that cochlear implants in this indication are not only effective but also cost-effective. The investigators' experimental protocol relies on real life therapeutic strategy, where a cochlear implant may be proposed once CROS and bone conductions systems have failed. Thus, all subjects enrolled in our study will try CROS and bone conduction devices. If these trials are ineffective, the remaining subjects will be randomized between two arms (cochlear implantation vs 6 months abstention followed by cochlear implantation). A comparative cost-utility analysis between the two arms, of medical consequences measured in terms of quality of life will identify a preference for a strategy. Specific binaural hearing measurements with respect to each treatment option (abstention, CROS, bone conduction device, cochlear implant) will also be collected.

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: 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.