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

Not Applicable
Suspended
Conditions
Superior Canal Dehiscence Syndrome
Vestibular Disorder
Registration Number
NCT05967065
Lead Sponsor
Region Stockholm
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

Detailed Description

Not available

Recruitment & Eligibility

Status
SUSPENDED
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients affected by certain vestibular disorders.

Exclusion Criteria

Patients with vertigo and dizziness without certain diagnosis.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
measure of eye movementsthrough study completion, an average of 18 months

angular velocity of eye movements during skull vibration.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Karolinska University Hospital, Hearing and Balance Unit

🇸🇪

Stockholm, Sweden

Karolinska University Hospital, Hearing and Balance Unit
🇸🇪Stockholm, Sweden
Luca Verrecchia, MD PhD
Contact
0046724654523
luca.verrecchia@ki.se

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