Diagnostic Precision Study on Vibration Induced Nystagmus Test for SCDS by Ortofone B250 Skull Vibration Protocol

Diagnostic Precision Study on Vibration Induced Nystagmus Test for SCDS by Ortofone

Status

Suspended

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05967065

Acronym

VIN by B250

Enrollment

Registered

2023-08-01

Start date

2023-07-20

Completion date

2025-12-31

Last updated

2025-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Superior Canal Dehiscence Syndrome, Vestibular Disorder

Brief summary

to study the videonystagmography response to a bone conducted vibration on the mastoid by B250 bone transducer in patients affected by vestibular loss, Menieres disease and Superior Semicircular Canal Dehiscence Syndrome vs healthy control subjects

Interventions

DIAGNOSTIC_TESTvibration induced nystagmus test

Vibration induced nystagmus test by bone transducer B250.

Study design

Allocation

NON_RANDOMIZED

Intervention model

PARALLEL

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 80 Years

Healthy volunteers

Yes

Inclusion criteria

Patients affected by certain vestibular disorders.

Exclusion criteria

Patients with vertigo and dizziness without certain diagnosis.

Design outcomes

Primary

Measure	Time frame	Description
measure of eye movements	through study completion, an average of 18 months	angular velocity of eye movements during skull vibration.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026