H81.0
Conditions
Interventions
Group 1: Observational study
This is a monocentric study. Data is collected from the routine diagnostics and visits from the Menière’s Disease outpatient clinic. Visits are performed every 3, 6, 9, or
Sponsors
Klinik und Poliklinik für Hals-Nasen-Ohrenheilkunde, LMU Klinikum
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: All patients with Menière's Disease who are treated in the neurotology outpatient clinic at the LMU Clinic and had given informed consent to participation in the study.
Exclusion criteria
Exclusion criteria: Vestibular migraines, other vestibular diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Observational Study Primary and secondary endpoints will be assessed at the respective treatment intervals 3, 6, 9, or 12 months. Primary endpoints: - Classification for the Menière categories: probable, definitive Menière’s Disease, Menière characteristica - Treatment result and complications of the different treatment options - Course of disease - Change in quality of life Secondary endpoints: - Estimation of prognosis - Contentment of patients - Doctor patient relation | — |
Secondary
| Measure | Time frame |
|---|---|
| Treatment scheme | — |
Countries
Germany
Contacts
Public ContactJennifer Spiegel
Klinik und Poliklinik für Hals-Nasen-OhrenheilkundeLMU Klinikum
Outcome results
None listed