Vestibular schwannoma treatment have an impact on the vestibular function of vestibular schwannoma patients. Our hypothesis is that surgery and radiotherapy will impair at a certain point after treatment the vestibular function, while the active…
ID
Bron
Verkorte titel
Aandoening
Unilateral vestibular schwannoma
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The vestibular function relating results to surgery, radiotherapy and active surveillance based on objective vestibular testing and dizziness related QoL
Achtergrond van het onderzoek
Currently the vestibular function is not well described in patients with unilateral vestibular schwannoma, nor is the effects of the different treatment modalities; surgery, radiotherapy or active surveillance. The vestibular symptoms such as dizziness, balance disturbance and/or vertigo are reported to have a major negative impact on the quality of life of the patients with vestibular schwannoma.
Hence, we aim to describe the vestibular function, function changes and dizziness related symptoms in vestibular schwannoma patients undergoing surgery, radiotherapy or active surveillance.
This study will increase our insight into the vestibular function and the impact of treatment strategy in this patient group. This in turn will help improve counselling of patients, enable adequate interventions if possible, and improve the quality of life of the patients with vestibular schwannoma.
Doel van het onderzoek
Vestibular schwannoma treatment have an impact on the vestibular function of vestibular schwannoma patients. Our hypothesis is that surgery and radiotherapy will impair at a certain point after treatment the vestibular function, while the active surveillance group will remain stable as long as the tumor size remains stable too.
Onderzoeksopzet
For the surgery group: before treatment, 5 to 7 days, 7 to 14 days, 1 month, 3 months, 6 to 12 months after surgery. For the radiotherapy group: before treatment, 6 weeks, 4 to 6 months, 1 year and 2 years after radiotherapy. For the active surveillance (wait and scan) group: baseline evaluation, 6 months, 12 months, 1 to 2 years.
Onderzoeksproduct en/of interventie
Surgery, radiotherapy and active surveillance (wait and scan)
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Aged 18 or older, being diagnosed with unilateral vestibular schwannoma, follow-up including either surgery, radiotherapy or active surveillance, able to provide a written informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Active additional neuro-otologic disorders, severe disability (e.g. neurological, cardiovascular, orthopedic, psychiatric), serious concurrent illness that might interfere with vestibular evaluation, patients under medical treatment that affects vestibular function.
Opzet
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Register | ID |
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NTR-new | NL9176 |
CCMO | NL74697.058.20 |
OMON | NL-OMON52093 |