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NCT05967065 Clinical Trial

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

Vestibular Disorder Clinical Trial

— VIN by B250  

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

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05967065
Other study ID # RegionStockholm
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 20, 2023
Est. completion date December 31, 2024

Study information
Verified date July 2023
Source Region Stockholm
Contact Luca Verrecchia, MD PhD
Phone +46724654523
Email luca.verrecchia@ki.se
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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

Recruitment information / eligibility
Status Recruiting
Enrollment 60
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: Patients affected by certain vestibular disorders. Exclusion Criteria: Patients with vertigo and dizziness without certain diagnosis.

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• vibration induced nystagmus test
Vibration induced nystagmus test by bone transducer B250.

Locations
Country Name City State
Sweden Karolinska University Hospital, Hearing and Balance Unit Stockholm

Sponsors (1)
Lead Sponsor Collaborator
Region Stockholm

Country where clinical trial is conducted

Sweden, 

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