Prospective Assessment of Peripheral-vestibular Function After Skull Base Surgery
NCT ID: NCT02773277
Last Updated: 2020-01-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2016-06-01
2019-05-31
Brief Summary
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Detailed Description
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The aim of this study is to characterize the frequency and pattern of iatrogenic peripheral-vestibular and cochlear hypofunction and to follow-up on the speed and extent of recovery. The investigators hypothesize that peripheral-vestibular and cochlear damage may be observed in a significant fraction of neurosurgical treatments in the posterior fossa including the cerebello-pontine angle. While initially deficits may be major, recovery is expected to be substantial or even complete due to peripheral restoration. As an important differential diagnosis, the investigators will evaluate also for potential (transient) cerebellar loss of function.
In order to quantify peripheral-vestibular function the investigators will use a CE-certified videooculography device to record responses to the head-impulse test before and in the days following elective skull base surgery. the video-head impulse test (vHIT) allows a quantitative video-based assessment of the functional integrity of all semicircular canals (MacDougall et al. 2013). By use of a high-speed video-camera mounted on goggles this test quantifies the vestibulo-ocular reflex (VOR), which is the fastest human reflex and allows the recognition and visual fixation of objects while head turns or ambulation. This test is used on a routine basis in our clinic and includes brief and fast, but small amplitude head turns (10-15° excursion) in the planes of the different semi-circular canals (SCCs). The SCCs are tested in three pairs in the horizontal, RALP (right anterior, left posterior) and LARP (left anterior, right posterior) plane (Weber et al. 2008). During testing the participant is asked to fixate a visual target straight ahead. Duration of this test: about 15 minutes.
Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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Single intervention arm
All patients will be assigned the intervention arm and will receive head-impulse testing before and in the days after skull base surgery.
head-impulse testing
all patients will receive quantitative head impulse testing using video goggles for all six semicircular canals.
Interventions
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head-impulse testing
all patients will receive quantitative head impulse testing using video goggles for all six semicircular canals.
Eligibility Criteria
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Inclusion Criteria
2. informed consent
Exclusion Criteria
2. disturbed consciousness
3. diagnosis of vestibular schwannoma
4. other neurological or systemic disorder which can cause dementia or cognitive dysfunction
5. known neck pain or status post neck trauma
18 Years
ALL
No
Sponsors
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University of Zurich
OTHER
Responsible Party
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Principal Investigators
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Niklaus Krayenbühl, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital Zurich, Neurology
Other Identifiers
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vHIT_surgery
Identifier Type: -
Identifier Source: org_study_id
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