Hearing loss pill tested on police officers fizzles out
NCT ID NCT04774250
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tested whether the epilepsy drug zonisamide could prevent hearing damage in police officers after shooting range training. Only 3 people enrolled before the study was stopped early. The goal was to see if the drug could reduce hearing loss measured by hearing tests and ear sound emissions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- zonisamide
- What this could lead to
- If it works, this could point toward a pill that protects hearing after sudden loud noise, like gunfire.
- What could go wrong
- The trial was terminated early with only 3 participants, so results are very limited. Zonisamide is an epilepsy drug and may cause side effects like dizziness or drowsiness.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
3 people
The number who actually took part.
- Started
-
Nov 2021
- Finished
-
Dec 2022
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Screening Inclusion Criteria: * Police officers who are scheduled for firearm training and/or certification on the range. * At least 18 years of age. * Air conduction thresholds are to be no worse than 25 dB HL from 0.5 kHz to 3 kHz, no worse than 30 dB HL at 4 kHz, and no worse than 45 dB HL at 6 and 8 kHz prior to shooting range exposure. * Ability to understand and willingness to sign an IRB approved written informed consent document. Enrollment Inclusion Criteria: * Observed audiometric TTS ≥ 10 dB HL at 2, 3, 4 and/or 6 kHz * Observed air-bone gap \< 10 dB HL at .5, 1, 2 and 4 kHz, with normal tympanometry Exclusion Criteria: * History of known sulfa allergy or hypersensitivity to carbonic anhydrase inhibitors. * History of moderate-to-severe kidney or liver disease. * Acute viral, bacterial, fungal or parasitic infection. * History of seizures. * Currently pregnant or breast-feeding. * Any current or history of otologic disorder. * History of ototoxic drug use. * Current use of strong/moderate 3A4 inhibitor/inducer and grapefruit juice. * For secondary outcomes, exclusion criteria is as follows: 1. DPOAE data will be used as a secondary outcome measure of TTS, and participants will be excluded if their DPOAE is absent at more than 3/7 frequencies. Criteria for a present response is any response that is \> 5 dB SPL above the noise floor and replicable within ±5 dB SPL. 2. ECochG: Participants will be excluded if the ECochG/ABR wave I response is absent. 3. WIN test: Participants with WIN scores greater than moderate difficulty or 14.9 dB SNR will be excluded.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Akron
Akron, Ohio, 44325-3001, United States
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