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Recruiting Not applicable NCT07420803

A Study Of Auricular Transcutaneous Vagus Nerve Stimulation In Chronic Dizziness

No applicable phase (e.g. observational)
Conditions: Chronic Dizziness Persistent Postural Perceptual Dizziness

Sponsor: Mayo Clinic

trial.available_in: БГ
Overview
The purpose of this study is to measure the change in dizziness, as measured by change in Dizziness Handicap Inventory (DHI) score, following a 4-week treatment period with auricular transcutaneous vagus nerve stimulation (aTVNS).
Who can participate
Inclusion Criteria: * Age 18-75, Persistent Postural-Perceptual Dizziness (PPPD) diagnosis per International Classification of Vestibular Disorders (ICVD). * Persistent dizziness ≥3 months and at least 1 dizziness exacerbation/day during 2-week run-in. * On stable medications/therapy for ≥4 weeks prior to baseline (if any). Exclusion Criteria: * Uncompensated peripheral/central vestibular deficit, sensory-afferent or cerebellar ataxia. * Cardiac disease (coronary disease, unstable arrhythmia), recurrent syncope (\>1 in past 12 months). * Neck surgery, vagotomy, or any condition interfering with vagal stimulation. * Pregnancy.
Interventions
Sham Device
OTHER
Auricular transcutaneous vagus nerve stimulation
OTHER
Locations 1
United States (1)
Mayo Clinic in Florida
Jacksonville , Florida
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
23.03.2026
Completion date
01.03.2027
Registry ID
NCT07420803
Source
clinicaltrials.gov
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