Relationship Between Degree of Hypofunction and Vestibular Tests in Patients With Vestibular Hypofunction

Medipol Health Group

Status: Enrolling

Conditions: Vestibular Assessment; Videonystagmography

Treatments: Diagnostic Test: Vestibular Hypofunction Group

Study type: Interventional

Funder types: Other

Identifiers

NCT06575946

VNG-VESTIBULAR TESTS

Details and patient eligibility

About

Patients with complaints of dizziness and balance problems will be included in the study. Inclusion criteria for the study are; being between the ages of 12-85, having a diagnosis of peripheral vestibular hypofunction. Exclusion criteria from the study are; not being able to communicate, having a diagnosis of central vestibulopathy and having mental disorders. Demographic information form, vestibular tests, balance tests will be used in the evaluation. The demographic information form includes demographic information (name, surname, gender, smoking, alcohol use, etc.) and clinical conditions (past illnesses and/or surgeries, medications used, whether there is a history of falls, if any, frequency, whether they are afraid of heights and uncomfortable in the dark, etc.). The patients will be diagnosed with videonystagmography (VNG) after the decision of the ENT physician, and the degree of hypofunction will be recorded. Vestibular and balance tests will be applied to the patients in a clinical setting. At the end of the study, it will be examined whether there is a relationship between the degree of vestibular hypofunction and the vestibular tests applied in the clinic.

Enrollment: 2,000 estimated patients

Sex: All

Ages: 12 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Being between 12-85 years old
• Having peripheral vestibular hypofunction
• Having good communication skills and participating in the work willingly

Exclusion criteria

• Having wavy vertigo
• Having mental retardation
• Failure to communicate
• Severely limited mobility
• Having acute Meniere's disease
• Having a neurological problem

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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2,000 participants in 1 patient group

Vestibular Hypofunction Group

Other group

Treatment:

Diagnostic Test: Vestibular Hypofunction Group