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Clinical Trials/NCT02532972
NCT02532972
Terminated
N/A

Cochlear Implantation for Treatment of Single-sided Deafness

Dr. Daniel Lee1 site in 1 country11 target enrollmentSeptember 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Total Unilateral Deafness
Sponsor
Dr. Daniel Lee
Enrollment
11
Locations
1
Primary Endpoint
Speech Perception Following Cochlear Implantation Assessed by Consonant-Nucleus-Consonant (CNC) Word Recognition Testing
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

This is a research study to determine whether a cochlear implantation (CI) device can improve hearing in people who are deaf in one ear (known as single-sided deafness).

Detailed Description

The goal of this study is to further investigate the role of CI in treating unilateral hearing loss and associated tinnitus. Single-sided deafness (SSD) afflicts approximately 60,000 new patients per year in the United States. The most common causes of these single-sided losses are sudden sensorineural hearing loss, Meniere's disease, trauma, and vestibular schwannoma. Patients with SSD face significant difficulty with communicating in the presence of background noise and in sound localization. Another significant problem for some SSD patients is tinnitus, which can be incapacitating and for which there are no therapies available that are considered to be of sufficient reliability to become a standard of care. Difficulty hearing in background noise and increased tinnitus can lead to significant frustration in social situations and contribute to increased isolation and a decreased quality of life. Treatment options for single sided deafness in the United States include contralateral routing of signals (CROS) hearing aids, bone-anchored hearing aids (BAHA) and use of assistive devices to improve the signal-to-noise in group situations. The first two devices take sound from the affected ear and transmit it to the unaffected ear. The last device consists of having a speaker wear a microphone and routing the signal directly to the patient's ear at a louder listening level. Although these devices can improve speech understanding in some patients, studies have shown that use of these devices does not ameliorate tinnitus or sound localization difficulties. Recent European studies have demonstrated that cochlear implantation (CI) can provide significant improvements in both perceived hearing ability and measured speech comprehension and localization in adult and pediatric patients with unilateral hearing loss. This suggests that CI may be a more effective option for this patient population than the CROS, BAHA or assistive devices.

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
April 25, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Dr. Daniel Lee
Responsible Party
Sponsor Investigator
Principal Investigator

Dr. Daniel Lee

Director, Pediatric Otology and Neurotology

Massachusetts Eye and Ear Infirmary

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older with the ability to provide informed consent
  • English as the primary language
  • Medically and psychologically suitable
  • Willing to receive/have received meningitis vaccinations
  • Able to pay for all care received through the study, either through the subject's insurance company or through self-pay
  • Able to comply with study requirements, including travel to the investigational sites
  • Severe to profound sensorineural hearing loss (≥70 dB HL (decibel hearing level) thresholds between 500 and 4000 Hz) in the worse ear with ≤ 20% Consonant-Nucleus-Consonant (CNC) word scores
  • Duration of single-sided deafness ≥ one year
  • Tinnitus localized to the affected ear, both ears, or in the head localized to the affected ear, both ears, or in the head
  • Expected subjects include those with:

Exclusion Criteria

  • Duration of single-sided deafness ≥ ten years
  • Pure tone thresholds ≥ 35 dB HL at 500, 1000, 2000, and 4000 Hz in the better ear
  • Consonant-Nucleus-Consonant (CNC) word scores ≤ 70% in the better ear
  • Chronic otitis media in either ear
  • Inner ear malformation in either ear
  • Autoimmune inner ear disease (fluctuation sensorineural hearing loss in either ear)
  • Evidence of retrocochlear pathology, including vestibular schwannoma
  • Unilateral tinnitus in the unaffected ear
  • Cochlear ossification
  • Demonstrated cognitive and/or developmental challenges

Outcomes

Primary Outcomes

Speech Perception Following Cochlear Implantation Assessed by Consonant-Nucleus-Consonant (CNC) Word Recognition Testing

Time Frame: Preop, 1-4 weeks, and 3, 6, and 12 months post-operatively

Ability to recognize words and sentences read by the tester from a set list at a loudness of 65 dB HL. The outcome is measured as a percent score of words recognized. The test takes place in a quiet environment.

Sound Detection Via Pure-tone Threshold Audiometry (PTA)

Time Frame: 3, 6 and 12 months post-operatively

Sound field thresholds following cochlear implantation via pure-tone threshold audiometry. Measured in dB HL (decibels hearing level) where a lower number means more sensitive hearing and a higher number means less sensitive hearing.

Secondary Outcomes

  • Subjective Changes in Tinnitus Following Cochlear Implantation Measured by Tinnitus Handicap Index (THI)(Preop and 12 months post-operatively)

Study Sites (1)

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