Vestibular function in the follow-up of patients with Vestibular Schwannoma (FUVES)
- Conditions
- vestibular functionvestibular schwannoma - acoustic neuroma10022396
- Registration Number
- NL-OMON52093
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 65
• aged 18 years or older
• being diagnosed with unilateral vestibular schwannoma
• with or without active VS treatment indication (i.e. RT, S or AS)
• with or without severe vestibular signs or symptoms
• able to provide a written informed consent
• active additional neuro- otologic disorders
• severe disability (e.g. neurological, cardiovascular, orthopedic,
psychiatric) or
• serious concurrent illness that might interfere with vestibular evaluation
• patients under medical treatment that affects the vestibular function
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The changes in objective vestibular test results and dizziness related QoL<br /><br>during follow-up. </p><br>
- Secondary Outcome Measures
Name Time Method <p>• To correlate the pre-operative vestibular function with the post-operative<br /><br>patient vestibular disability and handicap.<br /><br>• To correlate the irradiation dose-volume to the vestibular organs with<br /><br>vestibulo-toxicity after radiotherapy.<br /><br>• To correlate the natural development of the vestibular function over time in<br /><br>active surveillance.<br /><br>• To determine the effect of ITG in the vestibular function and vestibular<br /><br>complaints, with objective and subjective vestibular tests.<br /><br>• To correlate the questionnaires (DHI, PANQOL and SF-36) results with<br /><br>vestibular function.</p><br>