About this trial
The purpose of this study is to evaluate the vestibular effects of gamma-knife radiosurgery, as part of the treatment of vestibular schwannoma.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Men and women aged 18 to 90 included
Subject who benefited from gamma-knife radiosurgery as part of the treatment of vestibular schwannoma
Non-opposition of the subject to participate in the study
Affiliation to a French social security scheme or beneficiary of such a scheme
Disqualifiers
Subject with another vestibular pathology
Subject who did not benefit from a vestibular assessment before treatment with gamma-knife radiosurgery
Legal incapacity or limited legal capacity
Subject unlikely to cooperate in the study and/or weak cooperation anticipated by the investigator
Trial design
Single group
Treatments tested in this trial
Vestibular exam
Other interventionInterrogation, videonystagmoscopy, videonystagmography, video-head-impulse-test
Treatment groups
Trial outcomes
Primary outcomes
Description of vestibular function with videonystagmography before gamma-knife radiosurgery, as part of the treatment of vestibular schwannoma.
Videonystagmography: Results of caloric tests = Intervestibular deficit (in percentage)
Description of vestibular function with vidéonystagmoscopy before gamma-knife radiosurgery, as part of the treatment of vestibular schwannoma.
Videonystagmography: Results of caloric tests = Intervestibular deficit (in percentage)
Secondary outcomes
Description of vestibular symptoms before gamma-knife radiosurgery as part of the treatment of vestibular schwannoma.
Dizziness Handicap Inventoryquestionnaire (DHI questionnaire)
Description of vestibular symptoms after gamma-knife radiosurgery as part of the treatment of vestibular schwannoma.
Dizziness Handicap Inventoryquestionnaire (DHI questionnaire)
Sponsors and contacts
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