None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Adults 19 years of age or older - Patients who visited the hospital within 1 week of symptom onset - Patients with vestibular dysfunction observed in video oculography or video head impulse test - Patients with cerebral infarction confirmed by MRI in the cerebellum or brainstem - Patients who consented to participate in this study
Exclusion criteria
Exclusion criteria: - Patients with clinically serious diseases (liver disease, kidney disease, malignancy, etc.) - Patients who are unable to participate due to the judgment of other researchers - Those who do not agree to participate in the study - pregnant woman
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The vestibular ocular reflex gains and saccades-related variables obtained through video head impulse test, and the amplitude and latency of myoelectric potential obtained through the cervical vestibular evoked myopotential test | — |
Secondary
| Measure | Time frame |
|---|---|
| Subjective symptom questionnaire score(Dizziness Handicap Inventory, Visual Analogue Scale, EuroQol -5 Dimensions-5 Levels)) | — |
Countries
Korea, Republic of
Contacts
Pusan National University Hospital