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Prevention of Noise-induced Hearing Loss

Primary Purpose

Noise-induced Hearing Loss

Status
Withdrawn
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Zonisamide
Methylprednisolone
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Noise-induced Hearing Loss focused on measuring hearing loss, noise induced hearing loss, zonisamide

Eligibility Criteria

18 Years - 30 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • adults 18 to 30 years old
  • normal hearing
  • good to excellent health

Exclusion Criteria:

  • hearing loss
  • history of seizures
  • history of allergy or hypersensitivity to sulfonamide or oral steroid medications

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Zonisamide

Methylprednisolone

Control

Arm Description

Zonisamide 100 mg or 200 mg pill administered orally every day for 2 weeks

Methylprednisolone 32 mg or 64 mg pill administered orally once

no medication

Outcomes

Primary Outcome Measures

Pure Tone Thresholds
The primary outcome will be pure tone hearing thresholds (particularly 2000, 3000, 4000, and 6000 Hz) as measured by audiogram in a soundproof booth.

Secondary Outcome Measures

DPOAE
Distortion-product otoacoustic emissions (DPOAE) will be used as a secondary auditory outcome. A tinnitus questionnaire (Tinnitus Handicap Inventory) will be used to measure the secondary outcome of tinnitus, which frequently accompanies TTS.
Pure tone thresholds
This outcome measures recovery of hearing after loud music exposure

Full Information

First Posted
January 23, 2014
Last Updated
November 2, 2017
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT02049073
Brief Title
Prevention of Noise-induced Hearing Loss
Official Title
Zonisamide and Methylprednisolone to Prevent Noise-induced Temporary Hearing Loss
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Withdrawn
Why Stopped
new data makes this trial unethical
Study Start Date
October 31, 2017 (Actual)
Primary Completion Date
November 1, 2017 (Actual)
Study Completion Date
November 1, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Noise-induced hearing loss affects an estimated 5% of the worldwide population, with 30-40 million Americans exposed to hazardous sound or noise levels regularly. Sources of noise may be occupational, blast noise, or recreational. Trauma to the inner ear can occur through transient hearing loss or permanent hearing loss. Although hearing recovers after temporary transient hearing loss, growing evidence suggests that repeated temporary transient hearing loss may lead to a permanent hearing loss. Currently, there are no treatments and there are no known medications that can be used clinically to prevent noise-induced hearing loss in humans. The long-term goal of this research is to find medications that can prevent noise-induced hearing loss. The purpose of the present pilot study is to evaluate zonisamide and methylprednisolone as medications to prevent temporary transient hearing loss in humans.
Detailed Description
Noise-induced hearing loss (NIHL) affects an estimated 5% of the worldwide population, with 30-40 million Americans exposed to hazardous sound or noise levels regularly. Sources of noise may be occupational (e.g., manufacturing, construction), blast noise (e.g., firearms or explosions), or recreational (e.g., loud music, power tools). Trauma to the inner ear can occur through transient hearing loss (temporary threshold shifts, TTS) or permanent hearing loss (permanent threshold shift, PTS). Although hearing recovers after a TTS in about 24-48 hours, growing evidence suggests that repeated TTS may lead to PTS. Both TTS and PTS lead to a decrease in hearing thresholds at 3000 to 6000 Hz. Currently, there are no treatments for human NIHL although this is an area of active investigation. Protection against NIHL consists of limiting noise exposure through Occupational Safety and Health Administration (OSHA) limits to occupational noise and the wearing of hearing-protection devices (e.g., ear muffs or earplugs). There are no known medications that can be used clinically to prevent NIHL in humans. LePrell and colleagues have successfully established a protocol for inducing TTS using digitally-modified pop or rock music. This model of experimentally-induced TTS was intended to provide an ethical way of testing medications that might prevent NIHL. In a mouse model, Bao and colleagues were able to use zonisamide, an anti-epileptic medication approved for the treatment of partial seizures, and methylprednisolone, a glucocorticoid medication, to protect against noise-induced PTS. The long-term goal of this research is to find medications that can prevent NIHL. The goal of the present pilot study is to evaluate zonisamide and methylprednisolone as medications to prevent TTS in humans. Specific Aim 1: Examine zonisamide as a possible prophylactic medication to prevent noise-induced hearing loss, using an escalating dose protocol. Healthy volunteers would be given 100 or 200 mg of zonisamide as one-time doses or as a daily medication for two week (to establish a steady-state). They would be exposed to digitally-modified pop or rock music for 4 hours and undergo serial testing of hearing and monitoring for side effects after their sound exposure for 3-4 hours. They would be monitored at one day and one week post-exposure for hearing and other side effects. Hypothesis: Zonisamide is able to protect against noise-induced hearing loss in humans. Specific Aim 2: Examine methylprednisolone as a possible prophylactic medication to prevent noise-induced hearing loss, using an escalating dose protocol. Healthy volunteers would be given 32 or 64 mg of methylprednisolone as one-time doses. They would undergo the same music exposure and post-sound exposure monitoring as described above. Hypothesis: Methylprednisolone is able to protect against noise-induced hearing loss in humans

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Noise-induced Hearing Loss
Keywords
hearing loss, noise induced hearing loss, zonisamide

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Zonisamide
Arm Type
Experimental
Arm Description
Zonisamide 100 mg or 200 mg pill administered orally every day for 2 weeks
Arm Title
Methylprednisolone
Arm Type
Experimental
Arm Description
Methylprednisolone 32 mg or 64 mg pill administered orally once
Arm Title
Control
Arm Type
No Intervention
Arm Description
no medication
Intervention Type
Drug
Intervention Name(s)
Zonisamide
Other Intervention Name(s)
Zonegran
Intervention Description
Zonisamide 100 mg or 200 mg pill administered orally every day for 2 weeks
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone
Other Intervention Name(s)
Medrol, Solu-Medrol, Depo-Medrol, Hybrisil, A-Methapred
Intervention Description
Methylprednisolone 32 mg or 64 mg pill administered orally once
Primary Outcome Measure Information:
Title
Pure Tone Thresholds
Description
The primary outcome will be pure tone hearing thresholds (particularly 2000, 3000, 4000, and 6000 Hz) as measured by audiogram in a soundproof booth.
Time Frame
15 minutes post-music exposure
Secondary Outcome Measure Information:
Title
DPOAE
Description
Distortion-product otoacoustic emissions (DPOAE) will be used as a secondary auditory outcome. A tinnitus questionnaire (Tinnitus Handicap Inventory) will be used to measure the secondary outcome of tinnitus, which frequently accompanies TTS.
Time Frame
visit 2, pre-music exposure; visit 3-one week after music exposure
Title
Pure tone thresholds
Description
This outcome measures recovery of hearing after loud music exposure
Time Frame
1 hr 15 min, 2 hr 15 min, and 3 hr 15 min post exposure.
Other Pre-specified Outcome Measures:
Title
Pure tone thresholds
Description
Recovery of hearing after noise exposure
Time Frame
One week after music exposure.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: adults 18 to 30 years old normal hearing good to excellent health Exclusion Criteria: hearing loss history of seizures history of allergy or hypersensitivity to sulfonamide or oral steroid medications
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Judith Lieu, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
undecided

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Prevention of Noise-induced Hearing Loss

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