Noninvasive Therapy for Tinnitus
Noninvasive Therapeutic Hypothermia for Tinnitus
Restorear Devices LLC
40 participants
Nov 24, 2025
INTERVENTIONAL
Conditions
Summary
The goal of this interventional clinical study is to establish mild therapeutic hypothermia, delivered non-invasively to the structures of the inner ear, as a safe and repeatable therapeutic method for symptomatic relief of tinnitus. The study will assess both objective and subjective measures to address two main aims: 1. Ascertain the benefits of mild therapeutic hypothermia for symptomatic relief of chronic tinnitus in participants using the ReBound hypothermia device. 2. Ascertain the benefits of mild therapeutic hypothermia for symptom management in chronic tinnitus participants over six months using the ReBound device. Participants will wear the ReBound hypothermia device for 30 minutes in a single session. Researchers will compare results from those receiving the therapy to those from a control group (sham therapy). Participants will also use the device in-home for 6 months and monitor their symptoms with online surveys.
Eligibility
Inclusion Criteria4
- Adults aged 18 years or older at the time of signing the consent form
- Fluency in English or Spanish
- Chronic subjective tinnitus for more than 30 days defined as audible at least 75% of waking hours
- At least mild tinnitus, score ≥18 on the Tinnitus Handicap Inventory (THI)
Exclusion Criteria15
- Severe anxiety, score ≥ 15 on the Generalized Anxiety Disorder-7 (GAD-7)
- Tinnitus described as non-auditory or pulsatile in nature
- Catastrophic tinnitus, score ≥78 on the THI
- Tinnitus that is intermittent in nature
- Abnormal tympanometric findings
- Presence of conductive component as characterized by air-bone gaps ≥15 dB at two or more consecutive frequencies
- Otologic pathologies (including, but not limited to): acoustic neuroma/ vestibular schwannoma, chronic ear disease, Meniere's disease, documented fluctuating hearing loss, or ototoxicity
- Temporomandibular joint disorder
- Those who are currently receiving medical, pharmacologic, or therapeutic intervention for tinnitus or other otologic conditions.
- Active hearing aid use
- Dizziness at the time of signing the consent form or at the time of starting the study protocol treatment
- Adults unable to consent
- Individuals who are not yet adults (infants, children, teenagers)
- Pregnant women
- Prisoners
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Interventions
Mild therapeutic hypothermia (cooling), delivered non-invasively to the structures of the inner ear (cochlea) for 30 minutes, using headband-style proprietary device, ReBound.
Sham headband-style device. Participants assigned to use this device will be told they are receiving therapy for 30 minutes. However, no therapy is being provided.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07071480