CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 42 enrolled
Drug / intervention
Ketamine Hydrochloride in salinedrug
Likely dose
Ketamine Hydrochloride in saline 0.5 mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03336398
NCT03336398Phase 2Completed

Investigation of the NMDA Antagonist Ketamine as a Treatment for Tinnitus

New York State Psychiatric Institute·interventional·Posted Nov 8, 2017·Updated Mar 25, 2026

In Brief

A Phase 2 clinical trial evaluating Ketamine Hydrochloride in saline for Tinnitus. Completed, enrolled 42 participants across 1 site.

Detailed Summary

Tinnitus, or ringing in the ears, is a very common problem that often accompanies hearing loss. It affects up to 1 in 10 adults, and about 30% of people who experience chronic tinnitus find it very distressing. In these patients, symptoms of depression and anxiety often accompany tinnitus and there are no approved treatments. Clinical trials are ongoing to test a glutamate NMDA receptor antagonist (called esketamine), which is injected into the inner ear. However, the preliminary results with this medication show that it only works for tinnitus that results from acute injury. It does not treat tinnitus resulting from progressive hearing loss. Research in humans and animals suggest that the neurotransmitters glutamate and GABA are important in the development and maintenance of tinnitus. This data shows that over-activation of the NMDA receptor and a decrease in GABA signaling in the brain play a crucial role. Previous studies show that ketamine, which an antagonist at the NMDA receptor, increases GABA levels in the brain in participants with depression. Thus, in this experiment, this study will test the effect of ketamine on tinnitus, since it blocks the NMDA glutamate receptor and increase GABA levels. Two groups of participants will be included in this study: those who experience distress (symptoms of anxiety or depression) with tinnitus and those who have tinnitus but do not experience distress. Each participant will receive both ketamine and placebo on different days. Magnetic Resonance Spectroscopy (MRS) scans will be

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsTinnitus
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedNov 8, 2017
Enrollment StartSep 1, 2019
Primary CompletionJun 17, 2023
Study CompletionJul 1, 2024
TodayJul 2, 2026
Enrollment to primary: 3.8 yearsPosted 8.7 years ago

Interventions

Ketamine Hydrochloride in salinedrug

0.5 mg/kg IV of ketamine hydrochloride in saline will be administered with one of the MRS Scan