Gentamicin Treatment Prior to Schwannoma Surgery - No Residual Function

Sponsor
Lund University (Other)
Overall Status
Withdrawn
CT.gov ID
NCT02415257
Collaborator
(none)
0
1
2
65.1
0

Study Details

Study Description

Brief Summary

The purpose of the study is to determine whether vestibular and postural compensation following schwannoma surgery is improved by ablating vestibular function prior to surgery, even if vestibular function is absent according to modern assessment techniques

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Patients subjected to vestibular schwannoma surgery most often suffer from vertigo after surgery, even if no vestibular function can be found in pre-surgical assessment. According to retrospective data about 33% of patients scheduled for surgery do not have any measurable vestibular function. Even the occurrence of spontaneous nystagmus has been recorded in patients with no or very little function prior to surgery (Parietti-Winkler et al. 2008 JNNP). This indicates that despite new methods of measuring vestibular function, remaining vestibular function can be present and patients might benefit from pre-treatment of gentamicin (Tjernström et al. 2009 JNNP)

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Gentamicin Treatment Prior to Vestibular Schwannoma Surgery in Patients With no Measurable Remaining Vestibular Function
Study Start Date :
Apr 1, 2015
Actual Primary Completion Date :
Sep 1, 2020
Actual Study Completion Date :
Sep 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Gentamicin treated

Installation of gentamicin in the middle ear 6 weeks prior to surgery + rehabilitation exercises before and after both treatment and surgery. Rehabilitation exercises are not considered to be an intervention since their benign impact on vestibular/postural compensation is well documented and exclusion from exercises would not be approved by the ethical board

Drug: Gentamicin
Intratympanic installation of gentamicin 2-4 times depending on the efficacy of vestibular deafferentation
Other Names:
  • prehabituation
  • No Intervention: Non-gentamicin

    Rehabilitation exercises before and after both treatment and surgery Rehabilitation exercises are not considered to be an intervention since their benign impact on vestibular/postural compensation is well documented and exclusion from exercises would not be approved by the ethical board

    Outcome Measures

    Primary Outcome Measures

    1. Differences and changes of postural control following surgery, compared to before surgery [At first vestibular assessment at the time for inclusion and 6 months after surgery]

      Postural control assessed with posturography during a sensory conflict

    Secondary Outcome Measures

    1. Occurrence of spontaneous nystagmus after surgery [Day 1 after surgery and for the duration of either spontaneous nystagmus or hospital stay (up to 2 weeks)]

      To measure spontaneous nystagmus and its direction after surgery as a sign of vestibular deafferentation or central nervous damage

    2. Change of hearing levels [At first vestibular assessment and 4weeks after gentamicin installation]

      Measuring hearing levels (pure tone average and speech discrimination) before and after gentamicin treatment to determine possible detrimental effects on hearing

    3. Differences in the level of stress after surgery [Daily after surgery for the duration of the hospital stay, up to 2 weeks]

      Measuring cortisol in the saliva after surgery during the time patients are admitted to the hospital

    4. Differences of subjective well being after surgery [Immediate time after surgery (2weeks)]

      Daily subjective assessment of perceived vertigo/dizziness after surgery

    5. Differences of duration of hospital stay [After surgery for the duration of the hospital stay up to 2 weeks]

      Length of hospital stay required before patients can be discharged

    6. Differences of subjective well being after gentamicin treatment [Immediate time after gentamicin treatment (2weeks)]

      Daily subjective assessment of perceived vertigo/dizziness after gentamicin treatment

    7. Differences of perceived dizziness after surgery [6 months after surgery]

      Measurement of level of dizziness in daily life, questionnaire Dizziness Handicap Inventory (DHI)

    8. Differences of perceived anxiety/depression after surgery [6 months after surgery]

      Measurement of level of anxiety/depression in daily life, questionnaire Hospital Anxiety and Depression Scale (HADS)

    9. Change of level of perceived dizziness after surgery as compared to before surgery [At first vestibular assessment (inclusion) and 6 months after surgery]

      Measurement of level of dizziness in daily life, questionnaire Dizziness Handicap Inventory (DHI)

    10. Change of level of perceived anxiety/depression after surgery as compared to before surgery [At first vestibular assessment (inclusion) and 6 months after surgery]

      Measurement of level of anxiety/depression in daily life, questionnaire Hospital Anxiety and Depression Scale (HADS)

    11. Differences in vestibular compensation after surgery [6 months after surgery]

      Vestibular function tests; v-HIT (head impulse test), calorics and otolith tests to determine compensation and function after surgery

    12. Change of vestibular function after gentamicin treatment [6 weeks after gentamicin treatment]

      Vestibular function tests; v-HIT (head impulse test), calorics and otolith tests to determine compensation and function after gentamicin treatment

    Other Outcome Measures

    1. Differences of needed sick-leave from work and leisure activities [6 months after surgery]

      Time for return to normal daily activities after surgery, both job-related and leisure.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Vestibular schwannoma advised to surgical treatment

    • No measurable remaining vestibular function

    Exclusion Criteria:
    • impaired decision making

    • neurofibromatosis

    • signs for central dysfunction

    • remaining vestibular function

    • Patients are advised not to participate in the gentamicin arm if

    • hearing is better than 30 deciBel (dB) in pure tone average (500, 1000, 2000, 3-4000 Hz) and speech discrimination better than 70%

    • the neurosurgeon aim at hearing preservation surgery and do not want to risk gentamicin associated hearing loss

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Dept. OtoRhinoLaryngology Head and Neck Surgery, Skane University Hospital Lund Sweden 22185

    Sponsors and Collaborators

    • Lund University

    Investigators

    • Principal Investigator: Fredrik Tjernström, MD, PhD, Lund University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Lund University
    ClinicalTrials.gov Identifier:
    NCT02415257
    Other Study ID Numbers:
    • VS-FT-02
    First Posted:
    Apr 14, 2015
    Last Update Posted:
    Sep 11, 2020
    Last Verified:
    Sep 1, 2020

    Study Results

    No Results Posted as of Sep 11, 2020