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临床试验/NCT03533686
NCT03533686终止不适用

Comparative Study of Non-invasive Adhear Bone Conduction System to Traditional Bone Conduction Hearing Devices

University of Miami1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2018年4月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
66
试验地点
1
主要终点
Aided Hearing Thresholds for Conductive Hearing Loss

研究概览

简要总结

The purpose of this research study is to learn about the hearing outcomes of adult and pediatric patients who are treated with or are candidates for bone conductive devices (also termed "BAHA"). Hearing outcomes will also be assessed with a second audio processor device called the Adhear System.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Aims 1 and 2:
  • •Adult English speaking patients who are experienced users of Bone Anchored Implants (BAIs) for the indication of either single sided deafness or conductive hearing loss.
  • •Experienced will be defined as greater than 6 months of device use and no intermittent function of the device within 2 weeks of enrollment.
  • •Subjects will be limited to those who have normal hearing by bone conduction defined as a pure tone average of 25 dBHL or better at 500, 1000, 2000, & 3000 Hz in at least one ear.
  • •English speaking children 5 to 17 years of age and their primary guardian who present to the clinic for treatment by BAI on a headband device for the indications of single sided deafness or conductive hearing loss.
  • •Subjects will be limited to those who have no prior use of a BAI or bone conduction hearing device, normal hearing by bone conduction defined as a pure tone average of 25 dBHL or better at 500, 1000, 2000, & 3000 Hz in at least one ear. For those children where this cannot be definitively established, children will be included who display clinical signs of normal bone conduction hearing beyond a reasonable doubt and may include such evidence as (but not limited to): auditory brainstem response, speech awareness thresholds, visual reinforcement audiometry, conditioning play audiometry, CT scans, etc.)
  • •Aim 3 a & b:
  • •Pediatric bilateral or unilateral conductive hearing loss patients who are between the ages of 2 and 17 years of age
  • •Pediatric participants who are currently managed by the University of Miami with a bone conduction device attached to a softband.

排除标准

  • •Aims 1 & 2:
  • •Non-English speakers
  • •Participants reporting allergies to adhesives or highly reactive skin.
  • •Pediatric participants who are non-English speakers.
  • •Children who have previous experience with a BAI or bone conduction hearing device will not be included for study.
  • •Pediatric participants reporting allergies to adhesives or highly reactive skin.
  • •Aims 3a & 3b:
  • •Pediatric participants who are non-English speakers.
  • •Pediatric participants reporting allergies to adhesives or highly reactive skin.

研究组 & 干预措施

Single-Sided Deafness Adult (Aim1) Group

Experimental

Adult participants with single-sided deafness and are experienced bone conduction device users (6 months minimum of bone conduction device use and no intermittent use within the last 2 weeks) with an abutment implant will be provided with the Adhear system for 2 weeks (plus up to 90 days).

干预措施: Adhear Bone Conduction System (Device)

Conductive Hearing Loss Adult (Aim 2) Group

Experimental

Adult participants with conductive hearing loss and are experienced bone conduction device users (6 months minimum of bone conduction device use and no intermittent use within the last 2 weeks) with an abutment implant will be provided with the Adhear system for 2 weeks (plus up to 90 days).

干预措施: Adhear Bone Conduction System (Device)

Adhear followed by BAHA (Aim 3) Group

Experimental

Pediatric participants (aged 5-17 years) and their parents with conductive hearing loss or single-sided deafness who have not previously used a bone conduction device, will be provided with the Adhear system for 3 weeks (plus up to 90 days) followed by bone anchored hearing aid (BAHA) for another 3 weeks (plus up to 90 days).

干预措施: Adhear Bone Conduction System (Device)

Adhear followed by BAHA (Aim 3) Group

Experimental

Pediatric participants (aged 5-17 years) and their parents with conductive hearing loss or single-sided deafness who have not previously used a bone conduction device, will be provided with the Adhear system for 3 weeks (plus up to 90 days) followed by bone anchored hearing aid (BAHA) for another 3 weeks (plus up to 90 days).

干预措施: Bone anchored hearing aid (BAHA) (Device)

BAHA followed by Adhear (Aim 3) Group

Experimental

Pediatric participants (aged 5-17 years) and their parents with conductive hearing loss or single-sided deafness who have not previously used a bone conduction device, will be provided with the BAHA system for 3 weeks (plus up to 90 days) followed by Adhear for another 3 weeks (plus up to 90 days).

干预措施: Adhear Bone Conduction System (Device)

BAHA followed by Adhear (Aim 3) Group

Experimental

Pediatric participants (aged 5-17 years) and their parents with conductive hearing loss or single-sided deafness who have not previously used a bone conduction device, will be provided with the BAHA system for 3 weeks (plus up to 90 days) followed by Adhear for another 3 weeks (plus up to 90 days).

干预措施: Bone anchored hearing aid (BAHA) (Device)

Pediatric Unilateral Conductive Hearing Loss (Aim 3a) Group

Experimental

Pediatric participants (aged 2-17 years) and their parents with unilateral conductive hearing loss and are experienced bone conduction device users (6 months minimum of bone conduction device use) on a headband will be provided with the Adhear system for 2 weeks (plus up to 90 days).

干预措施: Adhear Bone Conduction System (Device)

Pediatric Bilateral Conductive Hearing Loss (Aim 3b) Group

Experimental

Pediatric participants (aged 2-17 years) and their parents with bilateral conductive hearing loss and are experienced bone conduction device users (6 months minimum of bone conduction device use) on a headband will be provided with the Adhear system. Participants who are fitted bilaterally will receive 2 Adhear systems (one for each ear) for 2 weeks (plus up to 90 days) at Visit 1. Participants who are fitted unilaterally will receive 1 Adhear system for 2 weeks (plus up to 90 days) at Visit 1, afterwards, will be fitted bilaterally at Visit 2 and receive the Adhear system for both ears for another 2 weeks (plus up to 90 days) for a total of 4 weeks (plus up to 180 days).

干预措施: Adhear Bone Conduction System (Device)

结局指标

主要结局

Aided Hearing Thresholds for Conductive Hearing Loss

时间窗: Day 14

Aided-hearing thresholds represent the softest sound that the participant can hear inside the audiometric test booth when using a hearing device. Aided hearing thresholds were measured using the participant's own device on a softband and the Adhear device in the test booth on day 14. Hearing thresholds were measured in hertz.

Aided Hearing Thresholds

时间窗: Day 14 of the intervention

Aided-hearing thresholds represent the softest sound that the participant can hear inside the audiometric test booth when using a hearing device. Aided hearing thresholds were measured using a traditional bone conduction device on a softband and the Adhear device in the test booth on day 14. Hearing thresholds were measured in hertz.

Aided Hearing Thresholds for Single Sided Deafness

时间窗: Day 14

Aided-hearing thresholds represent the softest sound that the participant can hear inside the audiometric test booth when using a hearing device. Aided hearing thresholds were measured using the participant's own device on a softband and the Adhear device in the test booth on day 14. Hearing thresholds were measured in hertz.

Aided Hearing Thresholds for Single Sided Deafness

时间窗: Day 1

Aided-hearing thresholds represent the softest sound that the participant can hear inside the audiometric test booth when using a hearing device. Aided hearing thresholds were measured using the participant's own device on their abutment and the Adhear device in the test booth on day 1. Hearing thresholds were measured in hertz.

Aided Hearing Thresholds for Conductive Hearing Loss

时间窗: Day 1

Aided-hearing thresholds represent the softest sound that the participant can hear inside the audiometric test booth when using a hearing device. Aided hearing thresholds were measured using the participant's own device on their abutment and the Adhear device in the test booth on day 1. Hearing thresholds were measured in hertz.

次要结局

  • Aided Speech in Noise Performance in Participants With Single-sided Deafness(Day 14)
  • Participant Satisfaction With BAHA (Aims 1, 2, 3a and 3b) or No Device (Aim 3)(Day 1)
  • Aided Speech-in-noise Performance in Participants With Single-sided Deafness(Day 1)
  • Participant Satisfaction With Adhear(Day 14)
  • Participant Satisfaction With Adhear at Day 28 (Aim 3b)(Day 28)
  • Aided Speech in Noise Performance in Participants With Conductive Hearing Loss(Day 14)
  • Aided Speech in Noise Performance in Participants With Conductive Hearing Loss(Day 1)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hillary A Snapp

Associate Professor

University of Miami

研究点 (1)

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