Benign Paroxysmal Positional Vertigo
Conditions
Interventions
Experimental group (Part III):None
Control group (Part III):None
Sponsors
Eye and ENT Hospital of Fudan University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Subjects voluntarily join the study and sign the informed consent form; 2. Age 18~70 years old; 3. Patients who are diagnosed with BPPV and undergo reduction therapy.
Exclusion criteria
Exclusion criteria: 1. Combination of balance dysfunction caused by other reasons (including cerebellar lesions, acoustic neuromas, vestibular neuritis, multiple sclerosis, etc.); 2. Patients who have limited head and neck movement or need head immobilization due to other reasons (severe cervical spondylosis, neck trauma, intracranial infection, etc.) and cannot complete follow-up; 3. Patients with serious systemic diseases, mental disorders, etc., who cannot complete follow-up; 4. The investigator believes that there are other reasons why he is not suitable to participate in this clinical study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Treatment outcome; | — |
Secondary
| Measure | Time frame |
|---|---|
| Recurrence rate;Clinical features;Vestibular Function Tests;Audiological Function Tests; | — |
Countries
China
Contacts
Public ContactLi Huawei; Wu Peixia
Eye and ENT Hospital of Fudan University
Outcome results
None listed